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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652720Generated: October 26, 2026

2-chloro-N-cyclopropylmethyl-N-[2-(3-phenyl1H-indol-2-yl)ethyl]acetamide → 2,3-dihydro-3-cyclopropylmethyl-11-phenyl-1H-[1,4]diazepino[1,7-a]indol-4(5H)-one

https://huagongshe.com/reaction/652720

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-chloro-N-cyclopropylmethyl-N-[2-(3-phenyl1H-indol-2-yl)ethyl]acetamideHCID 14210370—
CatalystBenzenemethanaminium, N,N,N-tributyl-, bromideHCID 2724282—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventSodium HydroxideHCID 14798—
Product2,3-dihydro-3-cyclopropylmethyl-11-phenyl-1H-[1,4]diazepino[1,7-a]indol-4(5H)-oneHCID 14210371—

Reaction Steps

A solution of 184.3 g 2-chloro-N-cyclopropylmethyl-N-[2-(3-phenyl-1H-indol-2-yl)ethyl]acetamide in 1843 ml methylene chloride is added dropwise under vigorous stirring to a suspension of 17.9 g N-benzyltributyl-ammoniumbromide in 1843 ml methylene chloride and 921 ml 30% sodium hydroxide. The mixture is stirred for further 10 minutes and diluted with 1 l water. The organic phase is separated, washed with water, dried and evaporated to dryness. The residue is dissolved in 500 ml boiling ethanol, cooled and treated with 500 ml ether. The resulting cristalline precipitate is filtered off, washed with ethanol/ather (1:1) and then ether to give 2,3-dihydro-3-cyclopropylmethyl-11-phenyl-1H-[1,4]diazepino[1,7-a]indol-4(5H)-one, m.p. 149°-150°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04673674
Source datasetuspto-grants-1987_06
ORD IDord-269af1cc43ba49e99273bb649c792914
Source noteuspto-grants-1987_06