Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 742971생성일: 2026년 10월 23일
Diisopropylethylamine → 3-methyl-6-[4-(tetrahydropyran-2-yloxy)butyl]-5,6,7,8-tetrahydro-1H-pyrido[4,3-d]pyrimidine-2,4-dione
https://huagongshe.com/ko/reaction/742971
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Lithium Bromide | HCID 82050 | — |
| 반응물 | 2H-Pyran, 2-(4-chlorobutoxy)tetrahydro- | HCID 170488 | — |
| 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-[4-(tetrahydropyran-2-yloxy)butyl]-5,6,7,8-tetrahydro-1H-pyrido[4,3-d]pyrimidine-2,4-dione | HCID 19423329 | 51% |
반응 단계
27 g of ethyldiisopropylamine, 18 g of lithium bromide and 46 g of 2-(4-chlorobutoxy) tetrahydropyran (86.3% pure according to GC) were added to 36.3 g of 3-methyl-5,6,7,8-tetrahydro-1H-pyrido[4,3-d]pyrimidine-2,4-dione in 1 l of dimethylformamide, with stirring, and the mixture was stirred for 5 h at 70° C. It was concentrated under reduced pressure and 34.5 g of crude 3-methyl-6-[4-(tetrahydropyran-2-yloxy)butyl]-5,6,7,8-tetrahydro-1H-pyrido[4,3-d]pyrimidine-2,4-dione were obtained after working-up of the residue by extraction with dichloromethane and water and after drying and concentration of the combined dichloromethane phases, and this crude product was purified by column chromatography on aluminum oxide (actiVity grade III) and elution with dichloromethane/ethanol (volume ratio 90:10).
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-7b2a6b2f8d0b47d7a07af6a44b1a050d |
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| 출처 메모 | uspto-grants-1996_09 |
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