참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Formaldehyde | HCID 712 | — |
| 반응물 | Carbon Disulfide | HCID 6348 | — |
| 반응물 | Methanesulfonic Acid | HCID 6395 | — |
| 반응물 | Morpholine | HCID 8083 | — |
| 반응물 | 2-Amino-4,6-dimethyl pyrimidine | HCID 13021 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 4,6-Dimethyl-2-(morpholin-4-ylthiocarbonylthiomethylamino)pyrimidine | HCID 53998646 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04764203 |
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| 출처 데이터셋 | uspto-grants-1988_08 |
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| ORD ID | ord-93a2ffbdfc7f40559b8be705008d4d29 |
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| 출처 메모 | uspto-grants-1988_08 |
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