반응식
[NH2:1][C:2]1[N:7]=[C:6]([NH2:8])[CH:5]=[C:4]([Cl:9])[N:3]=1.C([OH:12])C.C(OO)(=O)C>CC(OCC1C2C(=CC=CC=2)C(COC(C)=O)=C2C=1C=CC=C2)=O>[NH2:1][C:2]1[N+:7]([O-:12])=[C:6]([NH2:8])[CH:5]=[C:4]([Cl:9])[N:3]=1참가 물질
반응 조건
- 온도
- 35 °C
실험 절차
144.5 G. of 2,4-diamino-6-chloropyrimidine are suspended in 2000 ml. of ethanol. While stirring, the suspension is warmed to 35° C. (about 15 minutes), the greater part of the substance passing into solution. The mixture is then cooled to 6°-8° C. and, at this temperature, there are added dropwise within the course of 40 minutes 175 ml. of 40% peracetic acid in glacial acetic. After completion of the addition, the mixture is stirred at 6°-8° C. for a further 30 minutes. The mixture is then left to warm up to room temperature and stirred at this temperature for 3 hours. 2000 Ml. of petroleum ether are then added, the mixture is left to stir for 1 hour and then left to stand overnight. The separated precipitate is filtered off, back-washed with 200 ml. of petroleum ether and dried under reduced pressure, there being obtained 2,4-diamino-6-chloropyrimidine-3-oxide. Recrystallization yields analytically pure product, having a melting point of 193° C.
후처리
- temperatureThe mixture is then cooled to 6°-8° C. and, at this temperature, there
- additionare added dropwise within the course of 40 minutes 175 ml
- additionAfter completion of the addition
- stirringthe mixture is stirred at 6°-8° C. for a further 30 minutes
- waitThe mixture is then left
- temperatureto warm up to room temperature
- stirringstirred at this temperature for 3 hours
- waitthe mixture is left
- stirringto stir for 1 hour
- waitleft
- filtrationThe separated precipitate is filtered off
- washback-washed with 200 ml
- dry with materialof petroleum ether and dried under reduced pressure, there
출처 및 근거
- ORD 기록
- ord-40bc849c5eb9465eb24eb84deec4062d
- 출처 데이터셋
- uspto-grants-1979_11
- 특허 번호
- US04175189
연결된 노트
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