Ethyl orthoformate → HCID 20264251, compound
Reaction equation
[NH2:1][N:2]1[C:7](=[O:8])[CH:6]=[C:5]([CH3:9])[N:4]=[C:3]1[NH:10][NH2:11].[CH:12](OCC)(OCC)OCC>C(O)CCC>[NH2:11][N:10]1[C:3]2=[N:4][C:5]([CH3:9])=[CH:6][C:7](=[O:8])[N:2]2[N:1]=[CH:12]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A 2.4 g portion of 3-amino-2-hydrazino-6-methyl-4(3H)-pyrimidinone was dissolved in 100 ml of n-butanol by heating to the boiling point. A 20 ml portion of triethyl orthoformate was added and the solution was refluxed for 45 minutes. The solid was collected while the solution was hot, washed with ether and dried, giving 1.45 g of the desired intermediate, mp 202°-204°.
Workup
- temperatureby heating to the boiling point
- temperaturethe solution was refluxed for 45 minutes
- customThe solid was collected while the solution
- washwashed with ether
- customdried
Sources & evidence
- ORD record
- ord-f0a4b99aacb9439f8b4c8d7755bbaf66
- Source dataset
- uspto-grants-1985_10
- Patent number
- US04546181
Reaction notes
Loading…