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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 383995생성일: 2026년 10월 27일

Triethylamine → 4-oxo-4-(1-thien-2-yl-3,4-dihydroisoquinolin-2(1H)-yl)-N-(3-(trifluoromethyl)benzyl)butyric acid amide

https://huagongshe.com/reaction/383995

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-(Thiophen-2-yl)-1,2,3,4-tetrahydroisoquinolineHCID 2793643—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물4-Oxo-4-(3-(trifluoromethyl)benzylamino)butyric acidHCID 43397104—
용매TetrahydrofuranHCID 8028—
생성물4-oxo-4-(1-thien-2-yl-3,4-dihydroisoquinolin-2(1H)-yl)-N-(3-(trifluoromethyl)benzyl)butyric acid amideHCID 4682971087%

반응 단계

236 mg (1.1 mmol) of 1-(thiophen-2-yl)-1,2,3,4-tetrahydroisoquinoline, 380 mg (1.0 mmol) of HATU and 263 μl (1.9 mmol) of NEt3 were added in succession to a solution of 275 mg (1.0 mmol) of 4-oxo-4-(3-(trifluoromethyl)benzylamino)butyric acid (intermediate VVV01) in THF (8 ml) and the mixture was then stirred for 24 h at RT. Then it was diluted with EE (30 ml) and washed twice with a 4M aqueous NH4Cl solution and with a 1M aqueous NaHCO3 solution. The organic phase was dried over MgSO4, filtered and concentrated to small volume under vacuum. Column chromatography (EE) of the residue produced 410 mg (0.87 mmol, 87%) of 4-oxo-4-(1-thien-2-yl-3,4-dihydroisoquinolin-2(1H)-yl)-N-(3-(trifluoromethyl)benzyl)butyric acid amide. MS: m/z 473.1 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367700B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-0243b347ac7f47c39ca3b66c7569ab93
출처 메모uspto-grants-2013_02