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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1976257Generated: November 2, 2026

4-[(2-phenylbenzoyl)amino]benzoic Acid → HCID 12042762, compound

https://huagongshe.com/reaction/1976257

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[(2-phenylbenzoyl)amino]benzoic AcidHCID 10543502—
ReactantHCID 11858760HCID 11858760—
ProductHCID 12042762HCID 12042762—

Reaction Steps

The same procedures used in Example 25 were repeated using (11aS)-1,2,3,10,11,11a-hexahydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine prepared in Reference Example 28 and 4-[(2-phenylbenzoyl)amino]benzoic acid to give (11aS)-10-[4-[(2-phenylbenzoyl)amino]benzoyl]-1,2,3,10,11, 11a-hexahydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine. The resulting (11aS)-10-[4-[(2-phenylbenzoyl)amino]benzoyl]-1,2,3,10,11,11a-hexahydro-5H-pyrrolo[2,1-c][1,4]benzodiazepine was dissolved in ethyl acetate, a 4N hydrochloric acid-ethyl acetate solution was added thereto, the resulting precipitates were recovered through filtration and washed with a small amount of ethyl acetate to thus give the title compound. Yield 62.4%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06225306B1
Source datasetuspto-grants-2001_05
ORD IDord-4b20a95a4bd846a3a35ccfc68446e373
Source noteuspto-grants-2001_05