(3S,5R,8R,9S,10S,13S,14S)-16-Benzenesulfinyl-10,13-dimethyl-3-(tetrahydro-pyran-2-yloxy)-hexadecahydro-cyclopenta[a]phenanthren-17-one

Base Information

Chemical Name:(3S,5R,8R,9S,10S,13S,14S)-16-Benzenesulfinyl-10,13-dimethyl-3-(tetrahydro-pyran-2-yloxy)-hexadecahydro-cyclopenta[a]phenanthren-17-one
CAS No.:111263-94-6
Molecular Formula:C₃₀H₄₂O₄S
Molecular Weight:498.727
Hs Code.:

Synonyms:(3S,5R,8R,9S,10S,13S,14S)-16-Benzenesulfinyl-10,13-dimethyl-3-(tetrahydro-pyran-2-yloxy)-hexadecahydro-cyclopenta[a]phenanthren-17-one

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Chemical Property of (3S,5R,8R,9S,10S,13S,14S)-16-Benzenesulfinyl-10,13-dimethyl-3-(tetrahydro-pyran-2-yloxy)-hexadecahydro-cyclopenta[a]phenanthren-17-one

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Technology Process of (3S,5R,8R,9S,10S,13S,14S)-16-Benzenesulfinyl-10,13-dimethyl-3-(tetrahydro-pyran-2-yloxy)-hexadecahydro-cyclopenta[a]phenanthren-17-one

There total 3 articles about (3S,5R,8R,9S,10S,13S,14S)-16-Benzenesulfinyl-10,13-dimethyl-3-(tetrahydro-pyran-2-yloxy)-hexadecahydro-cyclopenta[a]phenanthren-17-one 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: 89.0%

: 670-98-4
methyl benzenesulfinate

: 111264-15-4
3β-hydroxy-5β-androstan-17-one 3-tetrahydropyranyl ether

: 111263-94-6
(3S,5R,8R,9S,10S,13S,14S)-16-Benzenesulfinyl-10,13-dimethyl-3-(tetrahydro-pyran-2-yloxy)-hexadecahydro-cyclopenta[a]phenanthren-17-one

Guidance literature:: With sodium hydride; In diethyl ether; for 4h; Ambient temperature;

Reference yield:

: 571-31-3
Epietiocholanolone

: 111263-94-6
(3S,5R,8R,9S,10S,13S,14S)-16-Benzenesulfinyl-10,13-dimethyl-3-(tetrahydro-pyran-2-yloxy)-hexadecahydro-cyclopenta[a]phenanthren-17-one

Guidance literature:: Multi-step reaction with 2 steps

1: p-toluenesulfonic acid / CH₂Cl₂

2: 89 percent / NaH / diethyl ether / 4 h / Ambient temperature

With sodium hydride; toluene-4-sulfonic acid; In diethyl ether; dichloromethane;

Reference yield:

: 110-87-2
3,4-dihydro-2H-pyran

: 111263-94-6
(3S,5R,8R,9S,10S,13S,14S)-16-Benzenesulfinyl-10,13-dimethyl-3-(tetrahydro-pyran-2-yloxy)-hexadecahydro-cyclopenta[a]phenanthren-17-one

Guidance literature:: Multi-step reaction with 2 steps

1: p-toluenesulfonic acid / CH₂Cl₂

2: 89 percent / NaH / diethyl ether / 4 h / Ambient temperature

With sodium hydride; toluene-4-sulfonic acid; In diethyl ether; dichloromethane;