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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1902197Generated: October 31, 2026

p-Chlorophenacyl bromide → HCID 12837734, compound

https://huagongshe.com/reaction/1902197

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Chlorophenacyl bromideHCID 68303—
ReactantHCID 12837720HCID 12837720—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 12837734HCID 12837734—

Reaction Steps

To the solution of 500 mg of 1,3,4,14b-tetrahydro-2H,10H-pyrazino[1,2-a]pyrrolo[2,1-c][1,4]benzodiazepine in 7.5 ml of dimethylformamide and 350 mg of triethylamine, 470 mg of α-bromo-p-chloroacetophenone are added and the mixture is stirred at room temperature for 2 hours. It is diluted with 60 ml of diethyl ether, washed with water, dried and evaporated. The residue is taken up in 15 ml of chloroform and the solution again evaporated, to yield the 2-(p-chlorobenzoyl-methyl)-1,3,4,14b-tetrahydro-10H-pyrazino[1,2-a]pyrrolo[2,1-c][1,4]benzodiazepine melting at 71°-74°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04362666
Source datasetuspto-grants-1982_12
ORD IDord-f70126e2712841279f58f7f3041e803c
Source noteuspto-grants-1982_12