Dimethylformamide → 4-Chloro-6-methoxy-7-((1-methylpiperidin-4-yl)methoxy)quinazoline
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH2:14][CH:15]1[CH2:20][CH2:19][N:18]([CH3:21])[CH2:17][CH2:16]1)[N:9]=[CH:8][NH:7][C:6]2=O.CN(C)C=O.S(Cl)([Cl:30])=O>>[Cl:30][C:6]1[C:5]2[C:10](=[CH:11][C:12]([O:13][CH2:14][CH:15]3[CH2:20][CH2:19][N:18]([CH3:21])[CH2:17][CH2:16]3)=[C:3]([O:2][CH3:1])[CH:4]=2)[N:9]=[CH:8][N:7]=1Participants
4
Procedure
A solution of 6-methoxy-7-((1-methylpiperidin-4-yl)methoxy)-3,4-dihydroquinazolin-4-one (2.8 g, 9.24 mmol) in thionyl chloride (28 ml) containing dimethylformamide (0.28 ml) was heated at reflux for 1 hour. The reaction was cooled, the volatiles were removed in vacuo and the resultant solid was triturated with diethyl ether, filtered, washed with diethyl ether and dried in vacuo. The solid was dissolved in dichloromethane and washed with saturated aqueous sodium hydrogen carbonate, water and brine. Evaporation of the solvent and drying in vacuo yielded 4-chloro-6-methoxy-7-((1-methylpiperidin-4-yl)methoxy)quinazoline (2.9 g, 98% yield):
Workup
- temperaturewas heated
- temperatureat reflux for 1 hour
- temperatureThe reaction was cooled
- customthe volatiles were removed in vacuo
- customthe resultant solid was triturated with diethyl ether
- filtrationfiltered
- washwashed with diethyl ether
- customdried in vacuo
- dissolutionThe solid was dissolved in dichloromethane
- washwashed with saturated aqueous sodium hydrogen carbonate, water and brine
- customEvaporation of the solvent
- customdrying in vacuo
Sources & evidence
- ORD record
- ord-ba20c0f9c9c546c0b8bab28a468ed375
- Source dataset
- uspto-grants-2007_06
- Patent number
- US07235559B1
Reaction notes
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