반응식
[CH3:1][C:2]1[N:7]=[C:6]([NH2:8])[C:5]([CH2:9][NH2:10])=[CH:4][N:3]=1.[C:11](=[O:13])=[O:12].C([OH:17])(C)C>>[C:11](=[O:17])([OH:13])[OH:12].[CH3:1][C:2]1[N:7]=[C:6]([NH2:8])[C:5]([CH2:9][NH2:10])=[CH:4][N:3]=1참가 물질
4
반응 조건
- 온도
- 10 °C
실험 절차
Into the same four-necked flask as used in Example 1 was charged a solution of 30.0 g (purity: 96.2 %, 0.209 mole) of crude 2-methyl-4-amino-5-aminomethylpyrimidine dissolved in 300 g of isopropanol, followed by maintaining the temperature of the solution at 10° C. Subsequently, 44 g (1 mole) of carbon dioxide was blown into the solution over about 2 hours and the reaction was carried out to precipitate a white crystal of 2-methyl-4-amino-5-aminomethylpyrimidine carbonate with extreme easiness. Then, the resulting crystal was filtered off, washed with a small amount of isopropanol, and dried in vacuo at 20° C. until it may have constant weight to obtain 37.8 g of 2-methyl-4-amino-5-aminomethylpyrimidine carbonate.
후처리
- customto precipitate a white crystal of 2-methyl-4-amino-5-aminomethylpyrimidine carbonate with extreme easiness
- filtrationThen, the resulting crystal was filtered off
- washwashed with a small amount of isopropanol
- customdried in vacuo at 20° C. until it
출처 및 근거
- ORD 기록
- ord-f40c41a4443949c4badc3c0ca9f5c6d3
- 출처 데이터셋
- uspto-grants-1991_08
- 특허 번호
- US05037982
연결된 노트
불러오는 중…