Technology Process of (3S,5S,9S,10R,13R,17S)-17-Cyano-3-(dimethyl-phenyl-silanyl)-10-formyl-4,4,13-trimethyl-1,7-dioxo-2,3,4,5,6,7,9,10,11,12,13,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-6-carboxylic acid allyl ester
There total 14 articles about (3S,5S,9S,10R,13R,17S)-17-Cyano-3-(dimethyl-phenyl-silanyl)-10-formyl-4,4,13-trimethyl-1,7-dioxo-2,3,4,5,6,7,9,10,11,12,13,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-6-carboxylic acid allyl ester which
guide to synthetic route it.
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synthetic route:
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908255-87-8
(3S,5S,9S,10R,13R,17S)-17-Cyano-3-(dimethyl-phenyl-silanyl)-10-formyl-4,4,13-trimethyl-1,7-dioxo-2,3,4,5,6,7,9,10,11,12,13,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-6-carboxylic acid allyl ester
- Guidance literature:
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With
caesium carbonate;
In
ethyl acetate;
at 20 ℃;
for 6h;
DOI:10.1021/jo0608725
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908255-87-8
(3S,5S,9S,10R,13R,17S)-17-Cyano-3-(dimethyl-phenyl-silanyl)-10-formyl-4,4,13-trimethyl-1,7-dioxo-2,3,4,5,6,7,9,10,11,12,13,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-6-carboxylic acid allyl ester
- Guidance literature:
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Multi-step reaction with 6 steps
1: 94 percent / N,N-diisopropylethylamine / CH2Cl2 / -78 - 20 °C
2: 70 percent / tributylamine; HCO2H; triphenylphosphine / Pd(OAc)2 / dimethylformamide / 1 h / 60 °C
3: 85 percent / KOH / methanol; H2O / 6 h / 20 °C
4: oxalyl chloride; DMF / toluene / 2 h / 20 °C
5: 0.548 g / LiHDMS / tetrahydrofuran; toluene / 0.33 h / -78 °C
6: 70 percent / Cs2CO3 / ethyl acetate / 6 h / 20 °C
With
potassium hydroxide; formic acid; oxalyl dichloride; tributyl-amine; caesium carbonate; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; triphenylphosphine; lithium hexamethyldisilazane;
palladium diacetate;
In
tetrahydrofuran; methanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jo0608725
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-
908255-87-8
(3S,5S,9S,10R,13R,17S)-17-Cyano-3-(dimethyl-phenyl-silanyl)-10-formyl-4,4,13-trimethyl-1,7-dioxo-2,3,4,5,6,7,9,10,11,12,13,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-6-carboxylic acid allyl ester
- Guidance literature:
-
Multi-step reaction with 7 steps
1: 90 percent / CH2Cl2; diethyl ether / 0.5 h / -78 °C
2: 94 percent / N,N-diisopropylethylamine / CH2Cl2 / -78 - 20 °C
3: 70 percent / tributylamine; HCO2H; triphenylphosphine / Pd(OAc)2 / dimethylformamide / 1 h / 60 °C
4: 85 percent / KOH / methanol; H2O / 6 h / 20 °C
5: oxalyl chloride; DMF / toluene / 2 h / 20 °C
6: 0.548 g / LiHDMS / tetrahydrofuran; toluene / 0.33 h / -78 °C
7: 70 percent / Cs2CO3 / ethyl acetate / 6 h / 20 °C
With
potassium hydroxide; formic acid; oxalyl dichloride; tributyl-amine; caesium carbonate; N-ethyl-N,N-diisopropylamine; N,N-dimethyl-formamide; triphenylphosphine; lithium hexamethyldisilazane;
palladium diacetate;
In
tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jo0608725