Sodium hydride → HCID 15490948, compound
Reaction equation
[CH2:1]([C:8]1[NH:9][C:10](=[O:15])[CH:11]=[C:12]([CH3:14])[N:13]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Br[CH2:17][CH2:18][O:19][C:20]1[CH:27]=[CH:26][C:23]([CH:24]=[O:25])=[CH:22][CH:21]=1.[H-].[Na+]>>[CH2:1]([C:8]1[N:9]([CH2:17][CH2:18][O:19][C:20]2[CH:27]=[CH:26][C:23]([CH:24]=[O:25])=[CH:22][CH:21]=2)[C:10](=[O:15])[CH:11]=[C:12]([CH3:14])[N:13]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
4
Procedure
The title compound (2.0 g, 20.6%) was prepared from 2-benzyl-4-methyl-1,6-dihydro-6-pyrimidone (5.6 g, 28.0 mmol), 4-[2-bromoethoxy]benzaldehyde (17.05 g, 30.1 mmol) in the presence of 95% NaH (873 mg, 35.0 mmol) as base by a similar procedure to that described in preparation 1.
Workup
- customthat described in preparation 1
Sources & evidence
- ORD record
- ord-444ccc272aaf4512bd12ba27685c168f
- Source dataset
- uspto-grants-1999_03
- Patent number
- US05885997
Reaction notes
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