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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418968Generated: November 1, 2026

Bromide ion → HCID 21842247, compound

https://huagongshe.com/reaction/1418968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantWaterHCID 962—
Reactanttert-Butyl peroxybenzoateHCID 11966—
ReactantHCID 54469685HCID 54469685—
SolventBenzeneHCID 241—
ProductHCID 21842247HCID 2184224747%

Reaction Steps

A solution of 6.80 g (0.0181 mol) of methyl (S)-2-(7-chloro-5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]-benzodiazepin-3-yl)-4,5-dihydro-oxazole-4-carboxylate in 700 ml of hot benzene was treated with 2.86 g (0.0199 mol) of copperl bromide and 5.1 ml (0.0272 mol) of tert-butyl perbenzoate according to the method described in Tetr. Letters 1994, 35, 2481. The mixture was boiled at reflux for 20 min., cooled and treated with 300 ml of water. The mixture was filtered, extracted with dichloromethane and chromatographed over silica gel with ethyl acetate as the eluent. There were obtained 3.15 g (47%) of methyl 2-(7-chloro-5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-3-yl)-oxazole-4-carboxylate as white crystals; m.p. 266°-268°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05885986
Source datasetuspto-grants-1999_03
ORD IDord-abac82e8b7d345fc99c37c0458ed2928
Source noteuspto-grants-1999_03