반응식
[NH2:1][C:2]1[N:7]=[C:6]([CH3:8])[CH:5]=[C:4]([CH3:9])[N:3]=1.[CH3:10][S:11]([OH:14])(=O)=[O:12].[C:15]1([CH3:25])[CH:20]=[CH:19]C=[C:17](S(O)(=O)=O)[CH:16]=1.[Na].[CH2:27]=O>O>[CH3:9][C:4]1[CH:5]=[C:6]([CH3:8])[N:7]=[C:2]([NH:1][CH2:27][S:11]([C:10]2[CH:19]=[CH:20][C:15]([CH3:25])=[CH:16][CH:17]=2)(=[O:14])=[O:12])[N:3]=1참가 물질
7
반응 조건
- 온도
- 90 °C
실험 절차
12.7 g (0.1 mole) of 2-amino-4,6-dimethylpyrimidine are suspended in 200 ml of water and then 9.7 g (0.1 mole) of methanesulfonic acid are stirred in to form a solution. To the stirred solution are added, in succession, 18.22 g (0.1 mole) of toluene-3-sulfonic acid, sodium salt, and 9.4 g (0.11 mole) of aqueous 35% formaldehyde. The mixture is stirred for 2 hours at room temperature and for another 30 minutes at 90° C. The colourless precipitate is filtered with suction after cooling and dried. Melting point: 191°-194° C. Yield: 25 g (86% of theory).
후처리
- customto form a solution
- filtrationThe colourless precipitate is filtered with suction
- temperatureafter cooling
- customdried
출처 및 근거
- ORD 기록
- ord-9ea8c5f23c574b2e8a2a3b12fa410e55
- 출처 데이터셋
- uspto-grants-1987_08
- 특허 번호
- US04685961
연결된 노트
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