5-benzoyl-2-benzyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole hydrochloride

Base Information

Chemical Name:5-benzoyl-2-benzyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole hydrochloride
CAS No.:1236142-54-3
Molecular Formula:C₂₅H₂₂N₂O*ClH
Molecular Weight:402.923
Hs Code.:

Synonyms:5-benzoyl-2-benzyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole hydrochloride

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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 5-benzoyl-2-benzyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole hydrochloride

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Technology Process of 5-benzoyl-2-benzyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole hydrochloride

There total 1 articles about 5-benzoyl-2-benzyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole hydrochloride 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: 67.0%

: 98-88-4
benzoyl chloride

: 6208-43-1
2-benzyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

: 1236142-54-3
5-benzoyl-2-benzyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole hydrochloride

Guidance literature:: 2-benzyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole; With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 0 ℃; Inert atmosphere;

benzoyl chloride; In N,N-dimethyl-formamide; mineral oil; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1016/j.bmc.2010.04.034

Reference yield: 90.0%

: 1236142-54-3
5-benzoyl-2-benzyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole hydrochloride

: 1236142-57-6
5-benzoyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indolehydrochloride

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; dichloromethane; at 20 ℃; for 48h; under 760.051 Torr;
DOI:10.1016/j.bmc.2010.04.034