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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethyl methanetricarboxylate | HCID 80471 | — |
| 반응물 | 5-(5-(Trifluoromethyl)pyridin-2-yl)-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridin-2-amine | HCID 73555049 | — |
| 용매 | O-Xylene | HCID 7237 | — |
| 생성물 | 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 | HCID 136337777 | 15.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08541430B2 |
|---|
| 출처 데이터셋 | uspto-grants-2013_09 |
|---|
| ORD ID | ord-2f262340c5794983a7389138666a2698 |
|---|
| 출처 메모 | uspto-grants-2013_09 |
|---|