Cyclopropanecarbonyl chloride → HCID 11695804, compound
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([C:23](Cl)=[O:24])[CH2:22][CH2:21]1>>[CH2:1]([C:3]1[N:7]=[C:6]([C:8]2[S:12][C:11]([NH:13][C:23]([CH:20]3[CH2:22][CH2:21]3)=[O:24])=[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]Participants
3
Procedure
Prepared from 5-(3-Ethyl-[1,2,4]oxadiazol-5-yl)-4-phenyl-thiazol-2-ylamine and cyclopropanecarbonyl chloride.
Sources & evidence
- ORD record
- ord-5551e08159fe4043afc165a04ec89249
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07910613B2
Reaction notes
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