Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38760생성일: 2026년 10월 24일
2-Methyl-2-thiopseudourea sulfate → Methyl 4-tert-butyl-2-(methylsulfanyl)pyrimidine-5-carboxylate
https://huagongshe.com/ko/reaction/38760
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2-Methyl-2-thiopseudourea sulfate | HCID 75270 | — |
| 반응물 | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| 반응물 | Methyl pivaloylacetate | HCID 99597 | — |
| 반응물 | Sodium Acetate | HCID 517045 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | Methyl 4-tert-butyl-2-(methylsulfanyl)pyrimidine-5-carboxylate | HCID 58168926 | — |
반응 단계
A mixture of methyl 4,4-dimethyl-3-oxopentanoate (10 g) and N,N-dimethyl formamide dimethyl acetal (9.5 mL) was stirred at 75° C. for 2 hours. To the reaction mixture were added N,N-dimethyl formamide (100 mL), S-methylisothiourea sulfate (2:1) (9.7 g), and sodium acetate (11.4 g), followed by stirring at 90° C. for 15 hours. The reaction mixture was cooled to room temperature, and water was added thereto. The aqueous layer was extracted with ethyl acetate and the organic layer was washed with water and saturated brine. The organic layer was dried over anhydrous magnesium sulfate, then filtered, and concentrated. The obtained residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate) to obtain methyl 4-tert-butyl-2-(methylsulfanyl)pyrimidine-5-carboxylate (8.4 g) as a colorless oily substance.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08524727B2 |
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| 출처 데이터셋 | uspto-grants-2013_09 |
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| ORD ID | ord-cf7b38d4db5847fe91ef4f679d98c286 |
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| 출처 메모 | uspto-grants-2013_09 |
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