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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354752Generated: October 26, 2026

2-Pyrrolidone → 7-amino-5-(o-chlorophenyl)-1,3-dihydro-1,3,3-trimethyl-2H-1,4-benzodiazepin-2-one

https://huagongshe.com/reaction/354752

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PyrrolidoneHCID 12025—
Reactant[5-(o-chlorophenyl)-2,3-dihydro-1,3,3-trimethyl-2-oxo-1H-1,4-benzodiazepin-7-yl]isocyanateHCID 20506146—
ReactantN-[5-(o-chlorophenyl)-2,3-dihydro-1,3,3-trimethyl-2-oxo-1H-1,4-benzodiazepin-7-yl]-1-pyrrolidinecarboxamideHCID 20506173—
SolventDiethylether ethylacetateHCID 21584169—
Product7-amino-5-(o-chlorophenyl)-1,3-dihydro-1,3,3-trimethyl-2H-1,4-benzodiazepin-2-oneHCID 20506178—

Reaction Steps

From 5.1 g (0.015 mol) of 7-amino-5-(o-chlorophenyl)-1,3-dihydro-1,3,3-trimethyl-2H-1,4-benzodiazepin-2-one and pyrrolidone there is obtained, in analogy to the details in Example 4, via [5-(o-chlorophenyl)-2,3-dihydro-1,3,3-trimethyl-2-oxo-1H-1,4-benzodiazepin-7-yl]isocyanate, N-[5-(o-chlorophenyl)-2,3-dihydro-1,3,3-trimethyl-2-oxo-1H-1,4-benzodiazepin-7-yl]-1 -pyrrolidinecarboxamide of melting point 248°-150° (ethyl acetate/ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04377522
Source datasetuspto-grants-1983_03
ORD IDord-8b4d3083e2e744a19d4e567ea2a65631
Source noteuspto-grants-1983_03