Ammonia → HCID 66665345, compound
Reaction equation
C[O:2][C:3]([C:5]1[CH:6]=[C:7]([O:38][CH3:39])[C:8]2[N:9]([C:11]([C:32]3[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=3)=[C:12]([C:14]3[CH:19]=[CH:18][C:17]([C:20]4([NH:24][C:25]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])=[O:26])[CH2:23][CH2:22][CH2:21]4)=[CH:16][CH:15]=3)[N:13]=2)[CH:10]=1)=O.[NH3:40]>CO>[C:28]([O:27][C:25](=[O:26])[NH:24][C:20]1([C:17]2[CH:16]=[CH:15][C:14]([C:12]3[N:13]=[C:8]4[C:7]([O:38][CH3:39])=[CH:6][C:5]([C:3](=[O:2])[NH2:40])=[CH:10][N:9]4[C:11]=3[C:32]3[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=3)=[CH:19][CH:18]=2)[CH2:21][CH2:22][CH2:23]1)([CH3:30])([CH3:29])[CH3:31]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 2-[4-(1-tert-butoxycarbonylamino-cyclobutyl)-phenyl]-8-methoxy-3-phenyl-imidazo[1,2-a]pyridine-6-carboxylic acid methyl ester (200 mg) and a solution of ammonia in methanol (7M, 2.65 mL) was heated at 120° C. for 6 hours under microwave irradiation. On cooling, the reaction mixture was concentrated in vacuo. Purification was achieved by chromatography on silica gel to give the title compound.
Workup
- temperatureOn cooling
- concentrationthe reaction mixture was concentrated in vacuo
- customPurification
Sources & evidence
- ORD record
- ord-5ca23228065a423c94adb7d4fbeee666
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08975265B2
Reaction notes
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