Triethyl orthoacetate → HCID 135703880, compound
Reaction equation
[OH:1][C:2]1[C:11]2[C:6](=[CH:7][C:8]([C:12]([NH:14][NH2:15])=[O:13])=[CH:9][CH:10]=2)[N:5]=[CH:4][N:3]=1.[C:16](OCC)(OCC)(OCC)[CH3:17]>>[CH3:16][C:17]1[O:13][C:12]([C:8]2[CH:7]=[C:6]3[C:11]([C:2](=[O:1])[NH:3][CH:4]=[N:5]3)=[CH:10][CH:9]=2)=[N:14][N:15]=1Participants
3
Procedure
4-Hydroxy quinazoline-7-hydrazide (0.41 g) was treated with triethyl orthoacetate (10 ml) at reflux under nitrogen for 24 hours. The mixture was cooled, filtered and purified by chromatography to give the title compound (0.09 g); m/z (M+1+) 229.
Workup
- temperatureat reflux under nitrogen for 24 hours
- temperatureThe mixture was cooled
- filtrationfiltered
- custompurified by chromatography
Sources & evidence
- ORD record
- ord-83f9acb7374d48189c780fa8fbda86f8
- Source dataset
- uspto-grants-2004_12
- Patent number
- US06828320B2
Reaction notes
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