Cyclopentylacetyl chloride → 2-Cyclopentyl-N-[5-(3-ethyl-[1,2,4]oxadiazol-5-yl)-4-phenyl-thiazol-2-yl]-acetamide
Reaction equation
[CH2:1]([C:3]1[N:7]=[C:6]([C:8]2[S:12][C:11]([NH2:13])=[N:10][C:9]=2[C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[O:5][N:4]=1)[CH3:2].[CH:20]1([CH2:25][C:26](Cl)=[O:27])[CH2:24][CH2:23][CH2:22][CH2:21]1>>[CH:20]1([CH2:25][C:26]([NH:13][C:11]2[S:12][C:8]([C:6]3[O:5][N:4]=[C:3]([CH2:1][CH3:2])[N:7]=3)=[C:9]([C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[N:10]=2)=[O:27])[CH2:24][CH2:23][CH2:22][CH2:21]1Participants
3
Procedure
Prepared from 5-(3-ethyl-[1,2,4]oxadiazol-5-yl)-4-phenyl-thiazol-2-ylamine and cyclopentyl-acetyl chloride.
Sources & evidence
- ORD record
- ord-95286e2ae14a442d913b56aeeb46246d
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07910613B2
Reaction notes
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