Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 742969생성일: 2026년 10월 24일
2-Chloroethyl methyl sulfide → 3-methyl-6-(2-methylsulfanylethyl)-5,6,7,8-tetrahydro-1H-pyrido[4,3-d]pyrimidine-2,4-dione
https://huagongshe.com/ko/reaction/742969
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Chloroethyl methyl sulfide | HCID 10965 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Lithium Bromide | HCID 82050 | — |
| 반응물 | 3-methyl-5,6,7,8-tetrahydro-1H-pyrido[4,3-d]pyrimidine-2,4-dione | HCID 10241423 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-methyl-6-(2-methylsulfanylethyl)-5,6,7,8-tetrahydro-1H-pyrido[4,3-d]pyrimidine-2,4-dione | HCID 19423333 | 45% |
반응 단계
36.3 g of 3-methyl-5,6,7,8-tetrahydro-1H-pyrido[4,3-d]-pyrimidine-2,4-dione, 23 g of 1-chloro-2-methylsulfanylethane (97% pure), 17.4 g of lithium bromide and 27 g of ethyldiisopropylamine in 700 ml of dimethylformamide were stirred for 14 h at 50° C. After the reaction mixture had been concentrated under reduced pressure, the residue was taken up with 400 ml of water and 400 ml, of dichloromethane, the pH was adjusted to 8 with sodium bicarbonate, with stirring, and the mixture was worked up by extraction with dichloromethane and water. 23 g of 3-methyl-6-(2-methylsulfanylethyl)-5,6,7,8-tetrahydro-1H-pyrido[4,3-d]pyrimidine-2,4-dione were obtained from the combined dichloromethane phases after drying, concentration and recrystallization of the residue from isopropanol.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05556854 |
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| 출처 데이터셋 | uspto-grants-1996_09 |
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| ORD ID | ord-82a2371955da43e1b96b6c197c37a35c |
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| 출처 메모 | uspto-grants-1996_09 |
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