(+)-(11S,11aS)-1,2,3,10,11,11a-hexahydro-9-(benzyloxy)-10-carbobenzyloxy-11-(3'-indolyl)-5H-pyrrolo<2,1-c><1,4>benzodiazepin-5-one

Base Information

Chemical Name:(+)-(11S,11aS)-1,2,3,10,11,11a-hexahydro-9-(benzyloxy)-10-carbobenzyloxy-11-(3'-indolyl)-5H-pyrrolo<2,1-c><1,4>benzodiazepin-5-one
CAS No.:125299-55-0
Molecular Formula:C₃₅H₃₁N₃O₄
Molecular Weight:557.649
Hs Code.:

Synonyms:(+)-(11S,11aS)-1,2,3,10,11,11a-hexahydro-9-(benzyloxy)-10-carbobenzyloxy-11-(3'-indolyl)-5H-pyrrolo<2,1-c><1,4>benzodiazepin-5-one

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Chemical Property of (+)-(11S,11aS)-1,2,3,10,11,11a-hexahydro-9-(benzyloxy)-10-carbobenzyloxy-11-(3'-indolyl)-5H-pyrrolo<2,1-c><1,4>benzodiazepin-5-one

Chemical Property:

Purity/Quality:

Safty Information:

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Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of (+)-(11S,11aS)-1,2,3,10,11,11a-hexahydro-9-(benzyloxy)-10-carbobenzyloxy-11-(3'-indolyl)-5H-pyrrolo<2,1-c><1,4>benzodiazepin-5-one

There total 13 articles about (+)-(11S,11aS)-1,2,3,10,11,11a-hexahydro-9-(benzyloxy)-10-carbobenzyloxy-11-(3'-indolyl)-5H-pyrrolo<2,1-c><1,4>benzodiazepin-5-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: 99.0%

: 120-72-9
indole

: 125299-57-2
(S)-9-Benzyloxy-11-hydroxy-5-oxo-2,3,11,11a-tetrahydro-1H,5H-benzo[e]pyrrolo[1,2-a][1,4]diazepine-10-carboxylic acid benzyl ester

: 125299-55-0
(+)-(11S,11aS)-1,2,3,10,11,11a-hexahydro-9-(benzyloxy)-10-carbobenzyloxy-11-(3'-indolyl)-5H-pyrrolo<2,1-c><1,4>benzodiazepin-5-one

Guidance literature:: In acetic acid; at 150 ℃; for 5h; Inert atmosphere; Sealed tube;
DOI:10.1074/jbc.M117.791558

Reference yield: 94.0%

: 120-72-9
indole

: 214277-31-3
(+)-(11aS)-1,2,3,10,11,11a-hexahydro-9-(benzyloxy)-10-(benzyloxycarbonyl)-11-hydroxy-5H-pyrrolo<2,1-c><1,4>benzodiazepin-5-one

: 125299-55-0
(+)-(11S,11aS)-1,2,3,10,11,11a-hexahydro-9-(benzyloxy)-10-carbobenzyloxy-11-(3'-indolyl)-5H-pyrrolo<2,1-c><1,4>benzodiazepin-5-one

Guidance literature:: With acetic acid; at 150 ℃; for 5h;
DOI:10.1021/jo972158g

Reference yield:

: 125299-56-1
(11aS)-1,2,3,10,11,11a-hexahydro-9-(benzyloxy)-10-(benzyloxycarbonyl)-5H-pyrrolo<2,1-c><1,4>benzodiazepin-5,11-dione

: 125299-55-0
(+)-(11S,11aS)-1,2,3,10,11,11a-hexahydro-9-(benzyloxy)-10-carbobenzyloxy-11-(3'-indolyl)-5H-pyrrolo<2,1-c><1,4>benzodiazepin-5-one

Guidance literature:: Multi-step reaction with 2 steps

1: 76 percent / NaBH₄, HCl / tetrahydrofuran; ethanol / 2 h / 0 °C

2: 94 percent / AcOH / 5 h / 150 °C

With hydrogenchloride; sodium tetrahydroborate; acetic acid; In tetrahydrofuran; ethanol;
DOI:10.1021/jo972158g