Ethyl orthoformate → HCID 21439072, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[CH:7][N:6]=[C:5]2[NH:12][NH2:13].[CH2:14](OC(OCC)OCC)C>>[Cl:1][C:2]1[CH:11]=[CH:10][C:9]2[N:8]=[CH:7][N:6]3[CH:14]=[N:13][N:12]=[C:5]3[C:4]=2[CH:3]=1Participants
3
Procedure
A mixture of 155.7 gms. of 6-chloro-4-hydrazinoquinazoline and 3000 ml. of triethoxy methane is refluxed with stirring for 48 hours, and after filtering off the insoluble material, the filtrate is evaporated in vacuo to dryness and the residue recrystallized from ether to obtain 9-chloro-1,2,4-triazolo[4,3-c]quinazoline, m.p. 179°-182° C.
Workup
- additionA mixture of 155.7 gms
- filtrationafter filtering off the insoluble material
- customthe filtrate is evaporated in vacuo to dryness
- customthe residue recrystallized from ether
Sources & evidence
- ORD record
- ord-39d749a37ba34979b5f286dbab538bf1
- Source dataset
- uspto-grants-1977_04
- Patent number
- US04020083
Reaction notes
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