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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2244289Generated: November 1, 2026

p-Chlorophenoxyacetyl chloride → 10-[(4-Chlorophenoxy)acetyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine

https://huagongshe.com/reaction/2244289

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Chlorophenoxyacetyl chlorideHCID 77771—
Reactant10,11-Dihydro-5H-benzo[e]pyrrolo[1,2-a][1,4]diazepineHCID 15547048—
Reactant10-[(4-Chloro-2-methylphenoxy)acetyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepineHCID 68681019—
Product10-[(4-Chlorophenoxy)acetyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepineHCID 68680429—

Reaction Steps

This compound was prepared from 10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine and 4-chlorophenoxyacetyl chloride in the same manner as the preparation of 10-[(4-chloro-2-methylphenoxy)acetyl]-10,11-dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine of Example 139, Step B, m.p. 120-122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07678787B2
Source datasetuspto-grants-2010_03
ORD IDord-e409af0b14b64b59a6187a3c016ba381
Source noteuspto-grants-2010_03