4-Morpholinecarbonyl chloride → HCID 10236928, compound
Reaction equation
[N:1]1([C:7](Cl)=[O:8])[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[NH2:10][CH2:11][CH2:12][CH2:13][CH2:14][N:15]1[C:23]2[C:22]([CH3:24])=[C:21]([CH3:25])[N:20]=[C:19]([NH2:26])[C:18]=2[N:17]=[CH:16]1>>[NH2:26][C:19]1[C:18]2[N:17]=[CH:16][N:15]([CH2:14][CH2:13][CH2:12][CH2:11][NH:10][C:7]([N:1]3[CH2:6][CH2:5][O:4][CH2:3][CH2:2]3)=[O:8])[C:23]=2[C:22]([CH3:24])=[C:21]([CH3:25])[N:20]=1Participants
3
Procedure
Using the method of Examples 16-26, 4-morpholinecarbonyl chloride was with 1-(4-aminobutyl)-6,7-dimethyl-1H-imidazo[4,5-c]pyridin-4-amine to provide red compound. The observed accurate mass was 347.2214.
Workup
- customto provide red compound
Sources & evidence
- ORD record
- ord-b362fe1206264e6b935a0c201daa288a
- Source dataset
- uspto-grants-2005_06
- Patent number
- US06903113B2
Reaction notes
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