2,2-Diphenylacetyl chloride → HCID 22661050, compound
Reaction equation
[CH2:1]([C:4]1[O:8][C:7]([NH2:9])=[N:6][CH:5]=1)[CH2:2][CH3:3].[C:10]1([CH:16]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:17](Cl)=[O:18])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>>[C:20]1([CH:16]([C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=2)[C:17]([NH:9][C:7]2[O:8][C:4]([CH2:1][CH2:2][CH3:3])=[CH:5][N:6]=2)=[O:18])[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=1Participants
3
Procedure
The title compound, white solid, m.p. 122° C. and MS: m/e=320.2 (M+) was prepared in accordance with the general method of example 44a from 5-propyl-oxazol-2-ylamine and 2,2-diphenylacetic acid chloride.
Sources & evidence
- ORD record
- ord-464093a75e9242eda6d7b5d71e8b8657
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06596743B2
Reaction notes
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