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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 639250Generated: October 27, 2026

Benzenebutanamine → 10-[(2-Methoxy-2'-methyl-1,1'-biphenyl-4-YL)carbonyl]-N-(4-phenylbutyl)-10,11-dihydro-5H-pyrrolo[2,1-C][1,4]benzodiazepine-3-carboxamide

https://huagongshe.com/reaction/639250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenebutanamineHCID 83242—
Reactant2,2,2-Trichloro-1-{10-[(2-methoxy-2'-methyl-1,1'-biphenyl-4-yl)carbonyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-3-yl}ethanoneHCID 16038825—
Product10-[(2-Methoxy-2'-methyl-1,1'-biphenyl-4-YL)carbonyl]-N-(4-phenylbutyl)-10,11-dihydro-5H-pyrrolo[2,1-C][1,4]benzodiazepine-3-carboxamideHCID 1603897261%

Reaction Steps

The title compound was prepared in the manner of Example 36 from 2,2,2-trichloro-1-{10-[(2-methoxy-2′-methyl-1,1′-biphenyl-4-yl)carbonyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-3-yl}ethanone of Example 35 and 4-phenylbutylamine. Purification was performed using HPLC with a normal phase column. Elution with a mixture of etoxynonafluorobutane and methanol gave the title compound (61% yield) as a yellow powder, m.p. 154-159° C. MS [(+)ESI, m/z]: 584 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691848B2
Source datasetuspto-grants-2010_04
ORD IDord-bcd3e0c38ff64fd8bfadd59a7efd74d0
Source noteuspto-grants-2010_04