Ammonia → HCID 11487261, compound
Reaction equation
C([NH:9][C:10]1[N:18]=[CH:17][N:16]=[C:15]2[C:11]=1[N:12]=[CH:13][N:14]2[C:19]([C@@H:21]([C@H:31]([CH2:44][OH:45])[O:32][CH2:33][P:34]([O:40][CH:41]([CH3:43])[CH3:42])([O:36][CH:37]([CH3:39])[CH3:38])=[O:35])[O:22]C(=O)C1C=CC=CC=1)=[O:20])(=O)C1C=CC=CC=1.N>CO>[N:18]1[C:10]([NH2:9])=[C:11]2[C:15]([N:14]([C:19]([C@@H:21]([C@H:31]([CH2:44][OH:45])[O:32][CH2:33][P:34]([O:40][CH:41]([CH3:43])[CH3:42])([O:36][CH:37]([CH3:39])[CH3:38])=[O:35])[OH:22])=[O:20])[CH:13]=[N:12]2)=[N:16][CH:17]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 11 (431 mg, 0.80 mmol) in MeOH saturated with ammonia (100 mL) was stirred at room temperature overnight. The mixture was concentrated, and the residue was purified by column chromatography (CH2Cl2:MeOH=9:1) to give compound 15 (278 mg, 0.67 mmol) as a white powder in 84% yield which was characterized as follows:
Workup
- concentrationThe mixture was concentrated
- customthe residue was purified by column chromatography (CH2Cl2:MeOH=9:1)
Sources & evidence
- ORD record
- ord-1b365df60728439f9fc524df2b7cfab3
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08501709B2
Reaction notes
Loading…