돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1877345생성일: 2026년 10월 25일

1,2,3,4-Tetrahydroquinoline → HCID 59294537, 화합물

https://huagongshe.com/reaction/1877345

반응식

참여 물질

역할이름HCID투입량
반응물1,2,3,4-TetrahydroquinolineHCID 69460—
반응물DiisopropylethylamineHCID 81531—
반응물2-(3-(Trifluoromethyl)phenoxy)-3-pyridinecarboxylic acidHCID 215891—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
용매DimethylformamideHCID 6228—
생성물HCID 59294537HCID 5929453756%

반응 조건

온도100 °C

반응 단계

To a solution of 2-(3-trifluoromethyl-phenoxy)-nicotinic acid (200 mg, 0.71 mmol, 1.0 equiv) in anhydrous DMF (3 mL) was added 1,2,3,4-tetrahydro-quinoline (113 mg, 107 μL, 0.85 mmol, 1.2 equiv; [CAS RN 635-46-1]), N-ethyldiisopropylamine (457 mg, 617 μL, 3.53 mmol, 5.0 equiv; [CAS RN 7087-68-5]) and HATU (322 mg, 0.85 mmol, 1.2 equiv; [CAS RN 148893-10-1]). The reaction mixture was heated by microwave irradiation to 100° C. for 5 min. Removal of the solvent mixture under reduced pressure and purification by preparative HPLC on reversed phase (Xterra® PrepMSC 18, 5 μm, 19×50 mm column equipped with a Gilson Liquid Handler 215 autosampler, two Rainin Dynamax® SD-300 pumps, a Sedex ELSD 75 lightscatter and a Dionex UVD 340S UV detector) eluting with a gradient of acetonitrile/water provided 157 mg (56%) of the title compound. MS (ISP): 399.2 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08309734B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-c4895d66e31e4ea58ff7b0350cb397f5
출처 메모uspto-grants-2012_11