반응식
[NH2:1][C:2]1[N:7]=[C:6](N)[N:5]=[C:4]([NH:9][CH:10]2[CH2:12][CH2:11]2)[N:3]=1.C(N([CH2:18][CH3:19])CC)C.[CH4:20].[O:21]1[CH2:25][CH2:24][CH2:23][CH2:22]1>>[CH:10]1([NH:9][C:4]2[N:3]=[C:2]([NH:1][C:22](=[O:21])[CH2:23][CH2:24][CH2:25][CH2:20][CH2:18][CH3:19])[N:7]=[CH:6][N:5]=2)[CH2:12][CH2:11]1참가 물질
5
실험 절차
To a suspension of 33.2 g of 2,4-diamino-6-cyclopropylamino-1,3,5-triazine and 30.3 g of triethylamine in 800 ml of tetrahydrofuran are slowly added dropwise, at 60° C., 50.9 g of oenanthic acid anhydride dissolved in 100 ml of tetrahydrofuran. The reaction mixture is subsequently stirred overnight at 60° C.; active charcoal is then added and the mixture is filtered hot. The filtrate is concentrated by evaporation, and isopropanol is added. The product is obtained, after filtration and drying, in the form of a white crystalline powder having a melting point of 195°-197° C.
후처리
- additionare slowly added dropwise, at 60° C.
- filtrationthe mixture is filtered hot
- concentrationThe filtrate is concentrated by evaporation, and isopropanol
- additionis added
- customThe product is obtained
- filtrationafter filtration
- customdrying, in the form of a white crystalline powder
출처 및 근거
- ORD 기록
- ord-ef5e7859ad19486db3974ffa43406063
- 출처 데이터셋
- uspto-grants-1989_04
- 특허 번호
- US04824845
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