(S)-1-[1-(2-hydroxypropyl)-9-(p-toluenesulfonyl)-1,3,4,9-tetrahydro-β-carbolin-2-yl]ethanone

Base Information

Chemical Name:(S)-1-[1-(2-hydroxypropyl)-9-(p-toluenesulfonyl)-1,3,4,9-tetrahydro-β-carbolin-2-yl]ethanone
CAS No.:633307-68-3
Molecular Formula:C₂₃H₂₆N₂O₄S
Molecular Weight:426.536
Hs Code.:

Synonyms:(S)-1-[1-(2-hydroxypropyl)-9-(p-toluenesulfonyl)-1,3,4,9-tetrahydro-β-carbolin-2-yl]ethanone

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (S)-1-[1-(2-hydroxypropyl)-9-(p-toluenesulfonyl)-1,3,4,9-tetrahydro-β-carbolin-2-yl]ethanone

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Technology Process of (S)-1-[1-(2-hydroxypropyl)-9-(p-toluenesulfonyl)-1,3,4,9-tetrahydro-β-carbolin-2-yl]ethanone

There total 5 articles about (S)-1-[1-(2-hydroxypropyl)-9-(p-toluenesulfonyl)-1,3,4,9-tetrahydro-β-carbolin-2-yl]ethanone 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%

: 75-16-1
methylmagnesium bromide

: 633307-67-2
(S)-[2-acetyl-9-(p-toluenesulfonyl)-2,3,4,9-tetrahydro-1H-β-carbolin-1-yl]acetaldehyde

: 633307-68-3
(S)-1-[1-(2-hydroxypropyl)-9-(p-toluenesulfonyl)-1,3,4,9-tetrahydro-β-carbolin-2-yl]ethanone

Guidance literature:: In tetrahydrofuran; diethyl ether; at 20 ℃; for 17h;
DOI:10.1021/ol030103x

Reference yield:

: 181218-86-0
(S)-1-allyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole

: 633307-68-3
(S)-1-[1-(2-hydroxypropyl)-9-(p-toluenesulfonyl)-1,3,4,9-tetrahydro-β-carbolin-2-yl]ethanone

Guidance literature:: Multi-step reaction with 5 steps

1: 98 percent / triethylamine / CH₂Cl₂ / 2 h / 20 °C

2: 45.3 percent / NaH / tetrahydrofuran / 23 h / 0 - 20 °C

3: OsO₄; N-methylmorpholine N-oxide / acetone; H₂O / 8.5 h / 20 °C

4: 216.8 mg / NaIO₄ / acetone; H₂O / 10 h

5: 85 percent / tetrahydrofuran; diethyl ether / 17 h / 20 °C

With sodium periodate; osmium(VIII) oxide; sodium hydride; 4-methylmorpholine N-oxide; triethylamine; In tetrahydrofuran; diethyl ether; dichloromethane; water; acetone;
DOI:10.1021/ol030103x

Reference yield:

: 633307-65-0
(S)-1-(1-allyl-1,3,4,9-tetrahydro-β-carbolin-2-yl)ethanone

: 633307-68-3
(S)-1-[1-(2-hydroxypropyl)-9-(p-toluenesulfonyl)-1,3,4,9-tetrahydro-β-carbolin-2-yl]ethanone

Guidance literature:: Multi-step reaction with 4 steps

1: 45.3 percent / NaH / tetrahydrofuran / 23 h / 0 - 20 °C

2: OsO₄; N-methylmorpholine N-oxide / acetone; H₂O / 8.5 h / 20 °C

3: 216.8 mg / NaIO₄ / acetone; H₂O / 10 h

4: 85 percent / tetrahydrofuran; diethyl ether / 17 h / 20 °C

With sodium periodate; osmium(VIII) oxide; sodium hydride; 4-methylmorpholine N-oxide; In tetrahydrofuran; diethyl ether; water; acetone;
DOI:10.1021/ol030103x