Thionyl Chloride → HCID 58574194, compound
Reaction equation
[CH3:1][N:2]1[C:11](=[O:12])[C:10]2[C:5](=[CH:6][C:7]([C:13]([OH:15])=O)=[CH:8][CH:9]=2)[N:4]=[CH:3]1.O=S(Cl)[Cl:18]>>[CH3:1][N:2]1[C:11](=[O:12])[C:10]2[C:5](=[CH:6][C:7]([C:13]([Cl:18])=[O:15])=[CH:8][CH:9]=2)[N:4]=[CH:3]1Participants
3
Procedure
A solution of 3-methyl-4-oxo-3,4-dihydroquinazoline-7-carboxylic acid (110 mg, 0.54 mmol) in SOCl2 (8 mL) was stirred at reflux for 5 h. The excess SOCl2 was then removed under reduced pressure. The crude 3-methyl-4-oxo-3,4-dihydroquinazoline-7-carbonyl chloride was used without further purification for the next step.
Workup
- temperatureat reflux for 5 h
- customThe excess SOCl2 was then removed under reduced pressure
- customThe crude 3-methyl-4-oxo-3,4-dihydroquinazoline-7-carbonyl chloride was used without further purification for the next step
Sources & evidence
- ORD record
- ord-2b2fc54978ef445085f81ea818a6fa78
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08772301B2
Reaction notes
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