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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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Thionyl ChlorideHCID 24386—
반응물2-Methyl-5,6-dihydro-1,4-oxathiine-3-carboxylic acidHCID 539946—
반응물1-Methylethyl 3-amino-4-fluorobenzoateHCID 21470256—
용매DichloromethaneHCID 6344—
생성물Isopropyl 4-fluoro-3-[(6-methyl-2,3-dihydro-1,4-oxathiine-5-carbonyl)amino]benzoateHCID 50730961%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05693827
출처 데이터셋uspto-grants-1997_12
ORD IDord-dc3f294f4b7d49ca97a6055435021b13
출처 메모uspto-grants-1997_12