Supporting Information:

Similar documents
The First Asymmetric Total Syntheses and. Determination of Absolute Configurations of. Xestodecalactones B and C

Supporting Information

Synthesis of Trifluoromethylated Naphthoquinones via Copper-Catalyzed. Cascade Trifluoromethylation/Cyclization of. 2-(3-Arylpropioloyl)benzaldehydes

Supporting Information. (1S,8aS)-octahydroindolizidin-1-ol.

Synthetic Studies on Norissolide; Enantioselective Synthesis of the Norrisane Side Chain

Supporting Information for Synthesis of C(3) Benzofuran Derived Bis-Aryl Quaternary Centers: Approaches to Diazonamide A

Photooxidations of 2-(γ,ε-dihydroxyalkyl) furans in Water: Synthesis of DE-Bicycles of the Pectenotoxins

An Efficient Total Synthesis and Absolute Configuration. Determination of Varitriol

Formal Total Synthesis of Optically Active Ingenol via Ring-Closing Olefin Metathesis

Supplementary Note 1 : Chemical synthesis of (E/Z)-4,8-dimethylnona-2,7-dien-4-ol (4)

Supporting Information

Supporting Text Synthesis of (2 S ,3 S )-2,3-bis(3-bromophenoxy)butane (3). Synthesis of (2 S ,3 S

Supporting Information

hydroxyanthraquinones related to proisocrinins

Supporting Information

Supporting Information

Supporting Information

Supporting Information. Table of Contents. 1. General Notes Experimental Details 3-12

A Meldrum s Acid-Derived Thione Dienophile in a Convergent and Stereoselective Synthesis of a Tetracyclic Quassinoid Intermediate

SYNTHESIS OF A 3-THIOMANNOSIDE

Synthesis of Cyclic Thioethers through Tandem C(sp 3 )- S and C(sp 2 )-S Bond Formations from α,β -Dichloro Vinyl Ketones

Supplementary Material for: Unexpected Decarbonylation during an Acid- Mediated Cyclization to Access the Carbocyclic Core of Zoanthenol.

Supporting Information

Qile Wang, and Nan Zheng* Department of Chemistry and Biochemistry, University of Arkansas. Fayetteville, Arkansas,

Synthesis of Simple Diynals, Diynones, Their Hydrazones, and Diazo Compounds: Precursors to a Family of Dialkynyl Carbenes (R 1 C C C C C R 2 )

SUPPLEMENTARY INFORMATION

Electronic Supplementary Material (ESI) for Chemical Communications This journal is The Royal Society of Chemistry 2012

Block: Synthesis, Aggregation-Induced Emission, Two-Photon. Absorption, Light Refraction, and Explosive Detection

A Mild, Catalytic and Highly Selective Method for the Oxidation of α,β- Enones to 1,4-Enediones. Jin-Quan Yu, a and E. J.

Supporting Information

Accessory Information

Enantioselective Organocatalytic Michael Addition of Malonate Esters to Nitro Olefins Using Bifunctional Cinchonine Derivatives

Total Synthesis of (±)-Vibsanin E. Brett D. Schwartz, Justin R. Denton, Huw M. L. Davies and Craig. M. Williams. Supporting Information

Supporting Information. for. Angew. Chem. Int. Ed. Z Wiley-VCH 2003

Supporting Information for

Divergent Synthesis of CF 3 -Substituted Polycyclic Skeletons Based on Control of Activation Site of Acid Catalysts

A Strategy Toward the Synthesis of C 13 -Oxidized Cembrenolides

Ring-Opening / Fragmentation of Dihydropyrones for the Synthesis of Homopropargyl Alcohols

Asymmetric Synthesis of Hydrobenzofuranones via Desymmetrization of Cyclohexadienones using the Intramolecular Stetter Reaction

SUPPORTING INFORMATION

Supporting Information

Enantioselective Synthesis of Fused Heterocycles with Contiguous Stereogenic Centers by Chiral Phosphoric Acid-Catalyzed Symmetry Breaking

Supporting Information

Synthesis of the α,β-unsaturated Aldehyde

Efficient Pd-Catalyzed Amination of Heteroaryl Halides

Aziridine in Polymers: A Strategy to Functionalize Polymers by Ring- Opening Reaction of Aziridine

Supporting Information

Domino reactions of 2-methyl chromones containing an electron withdrawing group with chromone-fused dienes

Supporting Information. Expeditious Construction of the DEF Ring System of Thiersinine B

Asymmetric 1,4-Reductions of Hindered β-substituted Cycloalkenones Using Catalytic CuH

Synthesis of Glaucogenin D, a Structurally Unique. Disecopregnane Steroid with Potential Antiviral Activity

Supporting Information

Preparation and ring-opening reactions of N- diphenylphosphinyl vinyl aziridines

Distyrylbenzene-aldehydes: identification of proteins in water. Supporting Information

Supporting Information

SUPPORTING INFORMATION. The "Aqueous" Prins Reaction

Synthesis of the C1-C10 Fragment of Madeirolide A

Supporting Information

Supporting Information

Photolysis for Vitamin D Formation. Supporting Information

Supporting Information

Synthesis of fluorophosphonylated acyclic nucleotide analogues via Copper (I)- catalyzed Huisgen 1-3 dipolar cycloaddition

Supporting Information

Supporting Information. for. Angew. Chem. Int. Ed. Z Wiley-VCH 2002

Organocatalytic asymmetric biomimetic transamination of aromatic ketone to optically active amine

Supplementary Information (Manuscript C005066K)

Supporting Information for

Opioid ligands with mixed properties from substituted enantiomeric N-phenethyl-5-

1G (bottom) with the phase-transition temperatures in C and associated enthalpy changes (in

SUPPLEMENTARY INFORMATION

SUPPLEMENTARY INFORMATION

Supporting Material. 2-Oxo-tetrahydro-1,8-naphthyridine-Based Protein Farnesyltransferase Inhibitors as Antimalarials

How to build and race a fast nanocar Synthesis Information

Supporting Information

SUPPORTING INFORMATION

Fast and Flexible Synthesis of Pantothenic Acid and CJ-15,801.

Supramolecular complexes of bambusuril with dialkyl phosphates

Supporting Information: Regioselective esterification of vicinal diols on monosaccharide derivatives via

Supporting Information

Total Syntheses of Aflavazole and 14-Hydroxyaflavinine

Electronic Supplementary Information

Supplementary Information

Facile Multistep Synthesis of Isotruxene and Isotruxenone

SUPPORTING INFORMATION

Supporting Information

Synthesis and Use of QCy7-derived Modular Probes for Detection and. Imaging of Biologically Relevant Analytes. Supplementary Methods

Chia-Shing Wu, Huai-An Lu, Chiao-Pei Chen, Tzung-Fang Guo and Yun Chen*

SUPPLEMENTARY INFORMATION

Carbonylative Coupling of Allylic Acetates with. Arylboronic Acids

Significant improvement of dye-sensitized solar cell. performance by a slim phenothiazine based dyes

Studies toward the Total Synthesis of Caribbean Ciguatoxin C-CTX-1: Synthesis of the LMN-Ring Fragment through Reductive Olefin Cross-Coupling

SUPPORTING INFORMATION. in the Synthesis of Fluorenones and ortho-arylated. Benzonitriles

Supporting Information for:

Supporting information. *Corresponding Author: Telephone number: , Fax number: ; address:

Eur. J. Org. Chem WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, 2006 ISSN X SUPPORTING INFORMATION

ELECTRONIC SUPPLEMENTARY INFORMATION. Modular Logic Gates: Cascading Independent Logic Gates via Metal Ion Signals

Supporting Information

Table of Contents for Supporting Information

Experimental details

Supporting Information

Transcription:

Enantioselective Synthesis of (-)-Codeine and (-)-Morphine Barry M. Trost* and Weiping Tang Department of Chemistry, Stanford University, Stanford, CA 94305-5080 1. Aldehyde 7. Supporting Information: CH 3 HC 7 To a solution of aldehyde 8 (110mg, 0.4mmol) in methylene chloride (4ml) was added trimetylsulfonium methyl sulfate (226mg, 1.2mmol) and 50% aqueous NaH (0.5ml) at 0 0 C. The reaction mixture was warmed to room temperature and stirred for 3h. Water (10ml) was added to the solution and the organic phase was separated. The aqueous phase was extracted with methylene chloride. The combined organic phase were washed with brine, dried over Na 2 S 4 and concentrated in vacuo. Flash column chromatography (25% ethyl acetate in pet ether) on flurosil provided 94mg (81%) of epoxide (dr=1:1). To a solution of epoxide (94mg, 0.33mmol) from previous step in THF (4ml) was added boron trifluoride etherate (20 µl, 0.16mmol). The solution was stirred at room temperature for 8h. Saturated sodium carbonate solution (10ml) was added to the reaction mixture. The solution was extracted with ethyl acetate (3x10ml). The combined organic phase was dried over Na 2 S 4 and concentrated in vacuo. Flash column chromatography (20%-40% ethyl acetate in pet ether) on flurosil provided 73mg (78%) of aldehyde. IR (neat) 2926, 2853, 2250, 1723, 1685, 1609, 1573, 1507, 1435, 1285, 1202, 1117, 1046, 1001, 804, 766, 725 cm -1. 1 H NMR (500MHz, C 6 D 6 ) δ 9.34 (t, J=2.5Hz, 1H), 6.40 S1

(d, J=8.3Hz, 1H), 6.27 (d, J=8.3Hz, 1H), 5.50 (ddd, J=4.0, 4.0, 10.0Hz, 1H), 5.31 (d, J=10.0Hz, 1H), 4.36 (dd, J=3.5, 6.0Hz, 1H), 3.33 (s, 3H), 3.10 (d, J=2.0Hz, 2H), 1.98 (d, J=17.0Hz, 1H), 1.93 (d, J=17.0Hz, 1H), 1.75-1.71 (m, 2H), 1.52-1.48 (m, 2H). 13 C NMR (125MHz, C 6 D 6 ) δ 198.01, 148.57, 145.36, 131.43, 130.90, 126.09, 124.07, 120.62, 116.74, 113.42, 85.22, 55.61, 48.20, 46.95, 27.44, 24.12, 19.98. HRMS: Calcd for C 17 H 17 N 3 (M + ): 283.1208, Found: 283.1210. 2. cis-bromoalkene 10. CH 3 Br 10 To a solution of carbontetrabromide (585mg, 1.76mmol) and triphenyl phosphine (923mg, 3.52mmol) in methylene chloride (10ml) was added a solution of aldehyde 6 (237mg, 0.88mmol) in methylene chloride (5ml) at 0 0 C. The reaction mixture was stirred at 0 0 C for 10min. The solution was filtered through a short silica gel pad and washed with ethyl acetate/pet ether (1:1). The organic solvent was removed in vacuo. Flash column chromatography (10-20% ethyl acetate in pet ether) provided 340mg (91%) of gem dibromoalkene. To a solution of gem dibromo alkene (275mg, 0.647mmol) from previous step and Pd(PPh 3 ) 4 (37mg, 0.032mmol) in toluene (7ml) was added a solution Bu 3 SnH (565mg, 1.94mmol) in toluene (0.5ml) via syringe pump in 20 min. The reaction was stopped after the addition was completed. Direct flash chromatography (5-20% ethyl acetate in pet ether) provided 197mg (88%) of colorless oil. [α] D = -71.9 (c=1.8, CHCl 3 ). IR (neat) 3076, 3022, 2930, 2841, 2251, 1619, 1573, 1503, 1423, 1284, 1204, 1115, 1071, 1046, 988, 912, 822, 718 cm -1. 1 H NMR (500MHz, CDCl 3 ) δ 7.16 (d, J=7.5Hz, 1H), 6.97 (dd, J=0.5Hz, J=8.5Hz, 1H), 6.81 (d, J=8.5Hz, 1H), 6.61 (d, J=7.5Hz, 1H), 6.04 (ddd, J=10.0, 5.0, 3.0Hz, 1H), 5.72 (d, J=10.0Hz, 1H), 4.85 (dd, J=3.5, 4.0Hz, 1H), 3.90 (s, 3H), 2.88 (d, J=17Hz, 1H), 2.80 (d, J=17Hz, 1H), 2.30- S2

2.22 (m, 2H), 2.12-1.98 (m, 2H). 13 C NMR (125MHz, CDCl 3 ) δ 146.80, 144.87, 131.18, 129.81, 129.26, 125.19, 124.22, 122.82, 116.72, 111.61, 110.74, 85.57, 55.87, 47.82, 27.22, 23.90, 19.57. HRMS: Calcd for C 17 H 16 79 BrN 2 (M + ): 345.0364, Found: 345.0358. 3. Heck cyclization product 14. CH 3 14 To a flask (10ml) was added cis-bromoalkene 10 (92mg, 0.266mmol), Pd(Ac) 2 (9mg, 0.04mmol), Ag 2 C 3 (221mg, 0.8mmol) and dppp (17mg, 0.04mmol). The flask was evacuated and filled with argon (3x). Degassed toluene (3ml) was added and the resulting suspension was heated at 107 0 C for 4h. Direct flash chromatography (5-15% ethyl acetate in petroleum ether) gave 46mg (65%) of product and 8mg (9%) recovered starting material. [α] D = +126.4 (c=0.73, CHCl 3 ). IR (neat) 3032, 2930, 2840, 2247, 1636, 1578, 1508, 1439, 1282, 1165, 1082, 808 cm -1. 1 H NMR (500MHz, CDCl 3 ) δ 6.73 (d, J=8.0Hz, 1H), 6.68 (d, J=8.0Hz, 1H), 6.50 (dd, J=9.5, 1.5Hz, 1H), 5.90 (dd, J=9.5, 5.5Hz, 1H), 5.69 (m, 1H), 5.47 (ddd, J=10.0, 4.5, 2.0Hz, 1H), 5.16 (dd, J=8.0, 4.5Hz, 1H), 3.89 (s, 3H), 3.33 (m, 1H), 2.68 (d, J=17Hz, 1H), 2.59 (d, J=17Hz, 1H), 2.65 (m, 1H), 2.22 (m, 1H). 13 C NMR (125MHz, CDCl 3 ) δ 145.51, 144.36, 126.93, 126.84, 124.51, 124.49, 123.70, 122.99, 118.34, 117.61, 113.55, 86.28, 56.33, 43.33, 37.44, 28.81, 25.42. HRMS: Calcd for C 17 H 15 N 2 (M + ): 265.1103, Found: 265.1099. 4. Enone 15. S3

CH 3 15 A flask (5ml) was charged with alkene 14(24mg, 0.09mmol), finely grounded Se 2 (11mg, 0.09mmol), oven dried quartz sand (50mg) and anhydrous dioxane (1ml). The solution was immersed in a 75 0 C oil bath. After stirring for 40 min, more selenium dioxide(11mg, 0.09mmol) was added. The solution was stirred for an additional 40min. A solution of Dess-Martin periodinane (115mg, 0.27mmol) in methylene chloride (0.7ml) was added to the above reaction mixture. The resulting solution was stirred at room temperature for 3h. Saturated sodium bicarbonate (5ml) was added and the solution was stirred for additional 30min. The organic phase was separated and the aqueous phase was extracted with ethyl acetate (2x10ml). The combined organic solvents were dried over Na 2 S 4 and concentrated in vacuo. The resulting slightly yellow oil was purified by flash chromatography (20% to 40% ethyl acetate in petroleum ether) to give 14.6 mg (58%) of the enone. [α] D = -34.4 (c=0.8, CHCl 3 ). IR (neat) 3040, 2949, 2841, 2243, 1678, 1637, 1506, 1456, 1438, 1279, 1103, 913, 813, 727 cm -1. 1 H NMR (500MHz, CDCl 3 ) δ 6.75 (s, 2H), 6.68 (dd, J=9.5, 1.8Hz, 1H), 6.60 (dd, J=10.5, 2.5Hz, 1H), 6.18 (dd, J=3.0, 10.5Hz, 1H), 5.91 (dd, J=6.0, 9.5Hz, 1H), 5.04 (s, 1H), 3.91 (s, 3H), 3.72 (m, 1H), 2.72 (d, J=17Hz, 1H), 2.65 (d, J=17Hz, 1H). 13 C NMR (125MHz, CDCl 3 ) 192.48, 145.33, 144.48, 144.32, 129.20, 126.42, 124.95, 123.03, 121.34, 119.80, 116.91, 115.20, 86.22, 56.70, 45.09, 37.27, 24.55. HRMS: Calcd for C 17 H 13 N 3 (M + ): 279.0895, Found: 279.0890. 5. amine 9. S4

CH 3 H 3 C N H 9 H To a cooled solution (-78 0 C) of enone 15 (20mg, 0.072mmol) in a mixed solvent of Et 2 (0.5ml) and CH 2 Cl 2 (0.5ml) was added 0.25ml of DIBAL (1M in hexane). After stirring at 78 0 C for 2h, the reaction mixture was warmed to 0 0 C and stirred for additional 1h. To the reaction mixture was added a solution of NH 4 Br (20mg, 0.2mmol) in 0.4ml of dry methanol followed by a 2M MeNH 2 solution (0.60ml) in methanol. The cooling bath was removed and the stirring was continued for 2h at room temperature. The mixture was cooled in an ice bath and 48mg (1.27 mmol) of NaBH 4 was added in three portions. The reaction mixture was stirred overnight at room temperature. The excess NaBH 4 was destroyed by addition of HCl (2M). The ph was adjusted to basic (ph>12) using 3N NaH. The resulting mixture was extracted with chloroform (6x10ml). The combined organic layer was dried over sodium sulfate and concentrated in vacuo. Flash column chromatography (5-10% MeH in CH 2 Cl 2 with 5% Et 3 N) provided 19mg of amine (89%). [α] D = -118.1 (c=0.7, CHCl 3 ). IR (neat) 3321, 3031, 2931, 2850, 1636, 1507, 1458, 1271, 1162, 1115, 1088, 799, 731 cm -1. 1 H NMR (500MHz, CDCl 3 ) δ 6.64 (d, J=8.0Hz 1H), 6.58 (d, J=8.0Hz, 1H), 6.50 (d, J=10.0Hz, 1H), 6.00 (dd, J=6.0, 9.5Hz, 1H), 5.80 (m, 1H), 5.29 (ddd, J=2.0, 3.0, 10.0Hz, 1H) 5.17 (dd, J=1.0, 6.5Hz, 1H), 4.23 (m, 1H), 3.85 (s, 3H), 2.82 (dd, J=3.0, 6.0Hz, 1H), 2.72 (ddd, J=16.1, J=11.1, 5.1Hz, 1H), 2.44 (ddd, J=15.5, 11.1, 5.4Hz, 1H), 2.37 (s, 3H), 2.28 (br, 1H), 2.15 (ddd, J=16.0, 10.5, 5.4Hz, 1H), 1.87 (ddd, 15.4, 10.4, 5.1Hz, 1H). 13 C NMR (125MHz, CDCl 3 ) δ 146.16, 143.76, 132.01, 129.15, 128.99, 127.59, 125.11, 123.74, 117.79, 111.99, 90.55, 66.02, 55.98, 47.81, 45.36, 37.69, 36.34, 35.83. HRMS: Calcd for C 18 H 21 N 3 (M + ): 299.1521, Found: 299.1528. 6. (-)-Codeine 2. To a cooled solution (-78 0 C) of amine 9 (7mg, 0.023mmol) in a mixed solvent of THF (1ml) and diisopropyl amine (0.2ml) was added 90µl of n-buli (0.135mmol, 1.5M S5

in hexane). The reaction mixture was warmed to room temperature and stirred for 6h under the irradiation of a 150W tungsten lamp at a distance of 0.5m. The solution was quenched with aqueous NaHC 3, dried over Na 2 S 4 and concentrated under vacuo. Flash column chromatography (5-10% MeH in CH 2 Cl 2 ) provided 4mg of codeine (57%). [α] D =-133(c=0.23, EtH) Lit 1 [α ] D = -137(c=1.15, EtH) Lit 2 [α ] D = +137.5(c=0.16, EtH, (+)-codeine). IR (neat) 3366, 2922, 2850, 1673, 1633, 1601, 1501, 1451, 1275, 1116, 1048, 786, 754 cm -1. 1 H NMR (500MHz, CDCl 3 ) δ 6.67 (d, J=8.0Hz, 1H), 6.58 (d, J=8.0Hz, 1H), 5.72 (ddd, J=1.5, 1.5, 10.0Hz, 1H), 5.29 (ddd, J=2.5, 2.5, 10.0Hz, 1H), 4.91 (dd, J=1.5, 7.0Hz, 1H), 4.19 (m, 1H), 3.85 (s, 3H), 3.44 (br s, 1H), 3.06 (d, J=18.5Hz, 1H), 2.79 (br s, 1H), 2.69 (m, 1H), 2.50 (s, 3H), 2.46 (m, 1H), 2.37 (dd, J=6.0, 18.5Hz, 1H), 2.15 (m, 1H), 1.90 (dd, J=1.5, 12.5Hz, 1H). 13 C NMR (125MHz, CDCl 3 ) δ 146.22, 142.36, 133.75, 130.60, 127.52, 126.22, 119.66, 112.93, 91.05, 66.20, 59.09, 56.28, 46.51, 42.75, 42.62, 40.10, 35.16, 20.63. In accordance with literature 2,3. (1) Gates, M.; Tschudi, G. J. Am. Chem. Soc. 1956, 78, 1380. (2) White, J. D.; Hrnciar, P.; Stappenbeck, F. J. rg. Chem. 1999, 64, 7871. (3) Carroll, F. I.; Moreland, C. G.; Brine, G. A.; Kepler, J. A. J. rg. Chem. 1976, 41, 996. S6