Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1938848생성일: 2026년 10월 25일
Triethylamine → Isopropyl 4-fluoro-3-[(6-methyl-2,3-dihydro-1,4-oxathiine-5-carbonyl)amino]benzoate
https://huagongshe.com/reaction/1938848
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | 2-Methyl-5,6-dihydro-1,4-oxathiine-3-carboxylic acid | HCID 539946 | — |
| 반응물 | 1-Methylethyl 3-amino-4-fluorobenzoate | HCID 21470256 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Isopropyl 4-fluoro-3-[(6-methyl-2,3-dihydro-1,4-oxathiine-5-carbonyl)amino]benzoate | HCID 507309 | 61% |
반응 단계
Thionyl chloride (4.6 g, 0.039 mole) was added to a stirred mixture of 5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxylic acid (6.0 g, 0.037 mole) and methylene chloride (50 ml). The mixture was warmed to 35°-40° C. for about 3 hours, then evaporated under reduced pressure. The residue, crude 5,6-dihydro-2-methyl-1,4-oxathiin-3-carbonyl chloride, was dissolved in methylene chloride (50 ml) and the ice-cooled solution treated dropwise with a solution of 1-methylethyl 3-amino-4-fluorobenzoate (7.4 g, 0.037 mole) and triethylamine (3.9 g, 0.039 mole) in methylene chloride (50 ml). The reaction mixture was stirred overnight at room temperature, and then washed in sequence with water (50 ml), dilute hydrochloric acid (3.5%, 50 ml), water (50 ml), dilute sodium hydroxide (2%, 25 ml) and water (50 ml), dried with anhydrous sodium sulfate and evaporated. Recrystallization of the solid residue from 100% ethanol (100 ml) gave light brown crystals, m.p. 132°-135° C. (7.8 g, 61% yield).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05693827 |
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| 출처 데이터셋 | uspto-grants-1997_12 |
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| ORD ID | ord-dc3f294f4b7d49ca97a6055435021b13 |
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| 출처 메모 | uspto-grants-1997_12 |
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