Formaldehyde → 4,6-Dimethyl-2-(morpholin-4-ylthiocarbonylthiomethylamino)pyrimidine

HRID 34865

반응식

HRID 34865 반응식
[OH-].[K+].[NH:3]1[CH2:8][CH2:7][O:6][CH2:5][CH2:4]1.[C:9](=[S:11])=[S:10].C=O.[NH2:14][C:15]1[N:20]=[C:19]([CH3:21])[CH:18]=[C:17]([CH3:22])[N:16]=1.[CH3:23]S(O)(=O)=O>O>[CH3:22][C:17]1[CH:18]=[C:19]([CH3:21])[N:20]=[C:15]([NH:14][CH2:23][S:10][C:9]([N:3]2[CH2:8][CH2:7][O:6][CH2:5][CH2:4]2)=[S:11])[N:16]=1

참가 물질

8

실험 절차

6.6 g (0.1 mole) of 85% potassium hydroxide and 8.9 g (0.1 mole) of morpholine are dissolved in 200 ml of water and, with cooling, 7.7 g (0.1 mole) of carbon disulfide are added. The mixture is stirred until a yellowish homogeneous solution is obtained. With cooling and stirring, 9.4 g (0.11 mole) of aqueous 35% formaldehyde and a solution of 12.7 g (0.1 mole) of 2-amino-4,6-dimethylpyrimidine and 9.7 g (0.1 mole) of methanesulfonic acid in 50 ml of water are added in succession. The reaction mixture is further stirred at room temperature, whereupon first an oil precipitates, which crystallises after a short time. After 24 hours the batch is diluted with 1 liter of water and the crystalline precipitate is filtered with suction and dried, affording 24 g (80% of theory) of the title compound with a melting point of 119°-121° C.

후처리

  1. temperaturewith cooling
  2. customis obtained
  3. temperatureWith cooling
  4. stirringstirring
  5. stirringThe reaction mixture is further stirred at room temperature
  6. customwhereupon first an oil precipitates
  7. customwhich crystallises after a short time
  8. additionAfter 24 hours the batch is diluted with 1 liter of water
  9. filtrationthe crystalline precipitate is filtered with suction
  10. customdried

출처 및 근거

ORD 기록
ord-93a2ffbdfc7f40559b8be705008d4d29
출처 데이터셋
uspto-grants-1988_08
특허 번호
US04764203

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