Tetrahydrofuran → 5-Amino-7,8-dihydro-2-(methylphenylamino)-7-oxopyrido[2,3-d]pyrimidine-6-carboxylic acid ethyl ester
반응식
[NH2:1][C:2]1[C:7]([C:8]#[N:9])=[CH:6][N:5]=[C:4]([N:10]([CH3:17])[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)[N:3]=1.C([CH:20]([C:24](Cl)=[O:25])[C:21](Cl)=[O:22])C.[O:27]1CC[CH2:29][CH2:28]1>>[CH2:28]([O:27][C:24]([C:20]1[C:21](=[O:22])[NH:1][C:2]2[N:3]=[C:4]([N:10]([CH3:17])[C:11]3[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=3)[N:5]=[CH:6][C:7]=2[C:8]=1[NH2:9])=[O:25])[CH3:29]참가 물질
4
실험 절차
To 10 g. (0.044 moles) of 4-amino-2-(methylphenylamino)-5-pyrimidine-carbonitrile in 200 ml. of tetrahydrofuran was added 6.7 g. (0.044 moles) of ethyl malonyl chloride and then this mixture was heated at reflux for 2 hours. The reaction was then filtered and the filtercake rinsed with tetrahydrofuran. The filtrate was evaporated to dryness on a rotary evaporator. The viscous liquid residue was treated with 50 ml. of 20% NaOH and heated to boiling for 5 minutes. The resulting solid was removed by filtration. This solid was slurried in water, acidified with acetic acid and filtered. The crude product was recrystallized from 95% ethanol to give 1.05 g. of solid with m.p. 297° C. (dec.).