Phenylacetylglycine → HCID 44578954, compound

Reaction equation

Cl.[Cl:2][C:3]1[CH:16]=[CH:15][C:6]([CH:7]([NH2:14])[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[CH:5][CH:4]=1.[C:17]1([CH2:23][C:24]([NH:26][CH2:27][C:28](O)=[O:29])=[O:25])[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[Cl:2][C:3]1[CH:4]=[CH:5][C:6]([CH:7]([NH:14][C:28]([CH2:27][NH:26][C:24](=[O:25])[CH2:23][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[O:29])[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[CH:15][CH:16]=1

Participants

Reactant 2

HCID 68144Phenylacetylglycine

HCID 162190964-Chlorobenzhydrylamine hydrochloride

Product 1

HCID 44578954HCID 44578954, compound

Procedure

Prepared in analogy to example 1.1 from rac-4-chlorobenzhydrylamine hydrochloride and phenylacetylamino-acetic acid (CA [500-98-1]).

Sources & evidence

ORD record: ord-2c57df4a564f4ee69fe4a7072b270f07
Source dataset: uspto-grants-2011_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07964645B2

Reaction notes

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