((3S,8S,9S,10R,13S,14S,16R,17S)-17-Acetyl-3-hydroxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-16-yl)-[4-(4-bromo-phenyl)-thiazol-2-yl]-acetonitrile

Base Information

Chemical Name:((3S,8S,9S,10R,13S,14S,16R,17S)-17-Acetyl-3-hydroxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-16-yl)-[4-(4-bromo-phenyl)-thiazol-2-yl]-acetonitrile
CAS No.:126354-20-9
Molecular Formula:C₃₂H₃₇BrN₂O₂S
Molecular Weight:593.628
Hs Code.:

((3S,8S,9S,10R,13S,14S,16R,17S)-17-Acetyl-3-hydroxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-16-yl)-[4-(4-bromo-phenyl)-thiazol-2-yl]-acetonitrile

Synonyms:((3S,8S,9S,10R,13S,14S,16R,17S)-17-Acetyl-3-hydroxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-16-yl)-[4-(4-bromo-phenyl)-thiazol-2-yl]-acetonitrile

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Chemical Property of ((3S,8S,9S,10R,13S,14S,16R,17S)-17-Acetyl-3-hydroxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-16-yl)-[4-(4-bromo-phenyl)-thiazol-2-yl]-acetonitrile

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Technology Process of ((3S,8S,9S,10R,13S,14S,16R,17S)-17-Acetyl-3-hydroxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-16-yl)-[4-(4-bromo-phenyl)-thiazol-2-yl]-acetonitrile

There total 2 articles about ((3S,8S,9S,10R,13S,14S,16R,17S)-17-Acetyl-3-hydroxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-16-yl)-[4-(4-bromo-phenyl)-thiazol-2-yl]-acetonitrile which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 85.0%

: 126354-16-3
(3β-acetoxypregna-5-en-20-on-16α-yl)cyanothioacetamide

: 99-73-0,132309-76-3
para-bromophenacyl bromide

: 126354-20-9
((3S,8S,9S,10R,13S,14S,16R,17S)-17-Acetyl-3-hydroxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-16-yl)-[4-(4-bromo-phenyl)-thiazol-2-yl]-acetonitrile

Guidance literature:: With potassium hydroxide; In ethanol; at 40 ℃;

Reference yield:

: 979-02-2
16-dehydropregnenolone acetate

: 126354-20-9
((3S,8S,9S,10R,13S,14S,16R,17S)-17-Acetyl-3-hydroxy-10,13-dimethyl-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-16-yl)-[4-(4-bromo-phenyl)-thiazol-2-yl]-acetonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: 72 percent / sodium ethoxide / ethanol / 1.5 h / Heating

2: 85 percent / 10percent aq. KOH / ethanol / 40 °C

With potassium hydroxide; sodium ethanolate; In ethanol;