Ethylamine → HCID 17981727, compound
Reaction equation
Cl[C:2]1[S:3][C:4]2[CH:10]=[C:9]([C:11]3[N:15]([CH:16]4[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]4)[CH:14]=[N:13][C:12]=3[C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[CH:8]=[CH:7][C:5]=2[N:6]=1.[CH2:28]([NH2:30])[CH3:29]>>[NH2:30][CH2:28][CH2:29][C:2]1[S:3][C:4]2[CH:10]=[C:9]([C:11]3[N:15]([CH:16]4[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]4)[CH:14]=[N:13][C:12]=3[C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[CH:8]=[CH:7][C:5]=2[N:6]=1Participants
3
Procedure
Beginning with 2-chloro-6-(1-(cyclohexyl)-4-(phenyl)-imidazol-5-yl)-benzothiazole and ethyl amine, prepare the title compound essentially as described in General Procedure B. MS(ES+): m/z=403.1 (M+H)+
Sources & evidence
- ORD record
- ord-04255346e0b841a19cb4a329b466a184
- Source dataset
- uspto-grants-2008_01
- Patent number
- US07320995B2
Reaction notes
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