1,1'-Carbonyldiimidazole → HCID 86296966, compound
Reaction equation
C1N=CN([C:6](N2C=NC=C2)=[O:7])C=1.[NH2:13][C:14]1[C:19]([NH2:20])=[CH:18][C:17]([C:21]2[C:22]([CH3:27])=[N:23][O:24][C:25]=2[CH3:26])=[CH:16][C:15]=1[C:28]([C:36]1[CH:41]=[CH:40][CH:39]=[CH:38][N:37]=1)([C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][N:31]=1)[OH:29]>C1COCC1.O.C(OCC)(=O)C>[CH3:27][C:22]1[C:21]([C:17]2[CH:16]=[C:15]([C:28]([OH:29])([C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][N:31]=3)[C:36]3[CH:41]=[CH:40][CH:39]=[CH:38][N:37]=3)[C:14]3[NH:13][C:6](=[O:7])[NH:20][C:19]=3[CH:18]=2)=[C:25]([CH3:26])[O:24][N:23]=1Participants
6
Reactant 2
Product 1
Reagents, catalysts & solvents 3
Procedure
CDI (1.1 g, 6 mmol) was added to a solution of (2,3-diamino-5-(3,5-dimethylisoxazol-4-yl)phenyl)di(pyridin-2-yl)methanol (1.43 g, 3.7 mmol) in THF (10 mL) and the reaction mixture was stirred for 3 days. The reaction mixture was diluted with 100 mL water and 100 mL ethyl acetate and sonicated and filtered to yield the desired product.
Workup
- customsonicated
- filtrationfiltered
Sources & evidence
- ORD record
- ord-206dc4a6b84749cba507317b2dfab6e6
- Source dataset
- uspto-grants-2016_02
- Patent number
- US09255089B2
Reaction notes
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