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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 383994생성일: 2026년 10월 26일

1,2,3,4-Tetrahydro-1-phenylisoquinoline → 4-oxo-4-(1-phenyl-3,4-dihydroisoquinolin-2(1H)-yl)-N-(3-(trifluoromethyl)benzyl)butyric acid amide

https://huagongshe.com/reaction/383994

반응식

참여 물질

역할이름HCID투입량
반응물1,2,3,4-Tetrahydro-1-phenylisoquinolineHCID 100137—
반응물CarbodiimideHCID 160435—
반응물Dichloromethane ethanolHCID 21584144—
반응물4-Oxo-4-(3-(trifluoromethyl)benzylamino)butyric acidHCID 43397104—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
생성물4-oxo-4-(1-phenyl-3,4-dihydroisoquinolin-2(1H)-yl)-N-(3-(trifluoromethyl)benzyl)butyric acid amideHCID 4621391662%

반응 단계

1.98 g (˜2.0 mmol) of PS carbodiimide resin were added to a solution of 209 mg (1.0 mmol) of 1-phenyl-1,2,3,4-tetrahydroisoquinoline and 275 mg (1.0 mmol) of 4-oxo-4-(3-(trifluoromethyl)benzylamino)butyric acid (intermediate VVV01) in a mixture of DCM and DMF (82 ml, 40:1 vv) and the mixture was shaken for 16 h at RT. Then the resin was filtered off and it was washed with DCM and MeOH. The filtrate was concentrated to small volume under vacuum. Column chromatography (DCM/EtOH 40:1) of the residue produced 287 mg (0.6 mmol, 62%) of 4-oxo-4-(1-phenyl-3,4-dihydroisoquinolin-2(1H)-yl)-N-(3-(trifluoromethyl)benzyl)butyric acid amide. MS: m/z 467.2 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367700B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-38e2fcc0283d45a5b68f1653fc06f081
출처 메모uspto-grants-2013_02