Ammonia → HCID 135763119, compound
Reaction equation
[OH:1][CH:2]([CH2:26][N:27]1[CH2:31][CH2:30][CH2:29][CH2:28]1)[CH2:3][O:4][C:5]1[CH:14]=[C:13]2[C:8]([C:9](=[O:23])[N:10](COC(=O)C(C)(C)C)[CH:11]=[N:12]2)=[CH:7][C:6]=1[O:24][CH3:25].N>CO>[OH:1][CH:2]([CH2:26][N:27]1[CH2:31][CH2:30][CH2:29][CH2:28]1)[CH2:3][O:4][C:5]1[CH:14]=[C:13]2[C:8]([C:9](=[O:23])[NH:10][CH:11]=[N:12]2)=[CH:7][C:6]=1[O:24][CH3:25]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
7-(2-Hydroxy-3-(pyrrolidin-1-yl)propoxy)-6-methoxy-3-((pivaloyloxy)methyl)-3,4-dihydroquinazolin-4-one (7.8 g) was stirred for 48 hours in a solution of methanol saturated with ammonia (200 ml). The solvent was evaporated and the solid obtained was washed with ether (2×) and ether/dichloromethane (95:5, 2×100 ml) to give the 7-(2-hydroxy-3-(pyrrolidin-1-yl)propoxy)-6-methoxy-3,4-dihydroquinazolin-4-one (5.5 g).
Workup
- customThe solvent was evaporated
- customthe solid obtained
- washwas washed with ether (2×) and ether/dichloromethane (95:5, 2×100 ml)
Sources & evidence
- ORD record
- ord-609e4199614a4160be6833b61ceeb91e
- Source dataset
- uspto-grants-2007_01
- Patent number
- US07160889B2
Reaction notes
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