2,2-Diphenylacetyl chloride → HCID 9797098, compound
Reaction equation
[CH:1]1([C:4]2[N:8]=[C:7]([NH2:9])[O:6][N:5]=2)[CH2:3][CH2:2]1.[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>>[CH:1]1([C:4]2[N:8]=[C:7]([NH:9][C:17](=[O:18])[CH:16]([C:10]3[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=3)[C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[O:6][N:5]=2)[CH2:3][CH2:2]1Participants
3
Procedure
The title compound, white solid, m.p. 163° C. and MS: m/e=219 (M+) was prepared in accordance with the general method of example 44a from 3-cyclopropyl-[1,2,4]oxadiazol-5-ylamine (Helv. Chim. Acta, 49(1966), 1430-1432) and 2,2-diphenylacetic acid chloride.
Sources & evidence
- ORD record
- ord-23154db51627459ba4016ce941ae3fe0
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06596743B2
Reaction notes
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