Iodoacetamide → HCID 54268875, compound
Reaction equation
I[CH2:2][C:3]([NH2:5])=[O:4].[NH:6]1[CH2:11][CH2:10][CH:9]([C:12]2[CH:17]=[CH:16][C:15]([C:18]3[N:23]=[C:22]([NH2:24])[CH:21]=[CH:20][CH:19]=3)=[CH:14][CH:13]=2)[CH2:8][CH2:7]1>>[C:3]([NH:5][N:6]1[CH2:11][CH2:10][CH:9]([C:12]2[CH:13]=[CH:14][C:15]([C:18]3[N:23]=[C:22]([NH2:24])[CH:21]=[CH:20][CH:19]=3)=[CH:16][CH:17]=2)[CH2:8][CH2:7]1)(=[O:4])[CH3:2]Participants
3
Procedure
Prepared from Example 13, using iodoacetamide to alkylate 6-[4-(piperidin-4-yl)-phenyl]-pyridin-2-ylamine, in 55%, mp 224-227° C.
Workup
- customPrepared from Example 13
Sources & evidence
- ORD record
- ord-e42795b3eab344f4bf1ccc07b1ee67bc
- Source dataset
- uspto-grants-2001_05
- Patent number
- US06235750B1
Reaction notes
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