Sodium Hydroxide → HCID 57409089, compound
Reaction equation
[CH3:1][C:2]1[N:3]=[C:4]([C:7]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[C:10](=O)[NH:9][N:8]=2)[S:5][CH:6]=1.P(Cl)(Cl)([Cl:20])=O.[OH-].[Na+]>>[Cl:20][C:10]1[C:11]2[C:16](=[CH:15][CH:14]=[CH:13][CH:12]=2)[C:7]([C:4]2[S:5][CH:6]=[C:2]([CH3:1])[N:3]=2)=[N:8][N:9]=1Participants
4
Procedure
A dry 50 mL RBF set up with stirring bar and reflux condenser was charged with 4-(4-methylthiazol-2-yl)phthalazin-1 (2H)-one (1.6 g, 6.6 mmol) and phosphorus oxychloride (7.4 ml, 78.9 mmol). The mixture was stirred under reflux for 18 hrs, then poured onto ice while stirring vigorously. To the iced mixture was added 6N NaOH until pH=9. Stirring was continued vigorously until solids formed. The solids were filtered, washed with water and dried in oven to afford 1-chloro-4-(4-methylthiazol-2-yl)phthalazine. MS m/z=262 [M+H]+. Calc'd for C12H8ClN3S: 261.7.
Workup
- temperaturereflux condenser
- stirringThe mixture was stirred
- temperatureunder reflux for 18 hrs
- additionpoured onto ice
- stirringwhile stirring vigorously
- stirringStirring
- customformed
- filtrationThe solids were filtered
- washwashed with water
- customdried in oven
Sources & evidence
- ORD record
- ord-8135356d11d245c393984ced5904bb6f
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07560551B2
Reaction notes
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