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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 44445생성일: 2026년 10월 24일

Triethyl methanetricarboxylate → 2-hydroxy-4-oxo-7-(5-trifluoromethyl-pyridin-2-yl)-5,6,7,8-tetrahydro-4H-9-thia-1,4a,7-triaza-fluorene-3-carboxylic acid ethyl ester

https://huagongshe.com/ko/reaction/44445

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참여 물질

역할이름HCID투입량
반응물Triethyl methanetricarboxylateHCID 80471—
반응물5-(5-(Trifluoromethyl)pyridin-2-yl)-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridin-2-amineHCID 73555049—
용매O-XyleneHCID 7237—
생성물2-hydroxy-4-oxo-7-(5-trifluoromethyl-pyridin-2-yl)-5,6,7,8-tetrahydro-4H-9-thia-1,4a,7-triaza-fluorene-3-carboxylic acid ethyl esterHCID 13633777715.5%

반응 조건

온도145 °C

반응 단계

The mixture of 5-(5-trifluoromethyl-pyridin-2-yl)-4,5,6,7-tetrahydro-thiazolo[5,4-c]pyridin-2-ylamine (5.7 gm, 0.019 mol) and triethyl methanetricarboxylate (16.1 ml, 0.076 mol) in xylene (100 ml) was heated at 140-150° C. for 6 hours. Xylene was evaporated and diethyl ether was then added and the suspension was stirred for 15 minutes. It was filtered and washed with ether. The crude solid was digested with dichloromethane (200 ml) and filtered to remove insoluble residue. Dichloromethane layer was distilled off under vacuum to give 1.3 gm of title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541430B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-2f262340c5794983a7389138666a2698
출처 메모uspto-grants-2013_09