2-Amino-5-chlorobenzophenone → HCID 178422575, compound

HRID 2053409Notes

Reaction equation

HRID 2053409 reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]([CH2:7][C:8]([OH:10])=O)[NH:5][N:6]=1.[NH2:11][C:12]1[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][C:13]=1[C:19]([C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)=O>>[Cl:18][C:15]1[CH:14]=[C:13]2[C:12](=[CH:17][CH:16]=1)[NH:11][C:8](=[O:10])[C:7]([C:4]1[NH:5][N:6]=[C:2]([CH3:1])[CH:3]=1)=[C:19]2[C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1

Participants

3

Reactant 2

HCID 128702-Amino-5-chlorobenzophenoneHCID 178425909HCID 178425909, compound

Product 1

HCID 178422575HCID 178422575, compoundYield 23%

Procedure

Synthesized from 5-methyl-2H-pyrazol-3-yl-acetic acid and (2-amino-5-chloro-phenyl)-phenyl-methanone according to general procedure 2. Yield 23%.

Sources & evidence

ORD record
ord-ef8267916bfe438c961e10112bff5aa7
Source dataset
uspto-grants-2008_02
Patent number
US07326788B2

Reaction notes

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