Acetic acid (3S,4R,5S,8R,9S,10R,13S,14S,17S)-17-acetoxy-4-(2-amino-phenylsulfanyl)-10,13-dimethyl-6-oxo-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester

Base Information

• Chemical Name: Acetic acid (3S,4R,5S,8R,9S,10R,13S,14S,17S)-17-acetoxy-4-(2-amino-phenylsulfanyl)-10,13-dimethyl-6-oxo-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester
• CAS No.: 174716-72-4
• Molecular Formula: C₂₉H₃₉NO₅S
• Molecular Weight: 513.698

Synonyms:Acetic acid (3S,4R,5S,8R,9S,10R,13S,14S,17S)-17-acetoxy-4-(2-amino-phenylsulfanyl)-10,13-dimethyl-6-oxo-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester

Chemical Property of Acetic acid (3S,4R,5S,8R,9S,10R,13S,14S,17S)-17-acetoxy-4-(2-amino-phenylsulfanyl)-10,13-dimethyl-6-oxo-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester

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Technology Process of Acetic acid (3S,4R,5S,8R,9S,10R,13S,14S,17S)-17-acetoxy-4-(2-amino-phenylsulfanyl)-10,13-dimethyl-6-oxo-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester

There total 1 articles about Acetic acid (3S,4R,5S,8R,9S,10R,13S,14S,17S)-17-acetoxy-4-(2-amino-phenylsulfanyl)-10,13-dimethyl-6-oxo-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester 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: 87.0%

3β,17β-diacetoxy-androst-4-en-6-one (3044-38-0) + 2-amino-benzenethiol (137-07-5) → Acetic acid (3S,4R,5S,8R,9S,10R,13S,14S,17S)-17-acetoxy-4-(2-amino-phenylsulfanyl)-10,13-dimethyl-6-oxo-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester (174716-72-4)

Guidance literature:

With sodium; In methanol; for 1.5h; Heating;

DOI:10.1139/v95-271

Reference yield: 58.0%

toluene-4-sulfonic acid (104-15-4) + Acetic acid (3S,4R,5S,8R,9S,10R,13S,14S,17S)-17-acetoxy-4-(2-amino-phenylsulfanyl)-10,13-dimethyl-6-oxo-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester (174716-72-4) → Acetic acid (3S,4R,5R,8R,9S,10R,13S,14S,17S)-17-acetoxy-10,13-dimethyl-6-oxo-4-[2-(toluene-4-sulfonylamino)-phenylsulfanyl]-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester

Guidance literature:

In benzene; for 2.5h; Heating;

DOI:10.1139/v95-271

Reference yield:

Acetic acid (3S,4R,5S,8R,9S,10R,13S,14S,17S)-17-acetoxy-4-(2-amino-phenylsulfanyl)-10,13-dimethyl-6-oxo-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester (174716-72-4) → Acetic acid (3S,4R,5R,8R,9S,10R,13S,14S,17S)-17-acetoxy-10,13-dimethyl-6-oxo-4-[2-(toluene-4-sulfonylamino)-phenylsulfanyl]-hexadecahydro-cyclopenta[a]phenanthren-3-yl ester

Guidance literature:

Multi-step reaction with 2 steps

1: 91 percent / p-toluene sulfonic acid / benzene / 3 h / Heating

2: 0.040 g / benzene / 2.5 h / Heating

With toluene-4-sulfonic acid; In benzene;

DOI:10.1139/v95-271

upstream raw materials:

3β,17β-diacetoxy-androst-4-en-6-one

2-amino-benzenethiol

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