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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 509783생성일: 2026년 10월 25일

Potassium Hydroxide → 8-Isopropyl-2-methyl-5-[2-(6-trifluoromethyl-pyridin-3-yl)-ethyl]-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

https://huagongshe.com/reaction/509783

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물5-Ethenyl-2-(trifluoromethyl)pyridineHCID 57416848—
반응물2,3,4,5-tetrahydro-8-isopropyl-2-methyl-1H-pyrido[4,3-b]indoleHCID 59455219—
용매N-methyl-2-pyrrolidoneHCID 13387—
용매Sodium chloride; waterHCID 57417360—
생성물8-Isopropyl-2-methyl-5-[2-(6-trifluoromethyl-pyridin-3-yl)-ethyl]-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indoleHCID 5787594098.5%

반응 단계

To a solution of 8-Isopropyl-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (0.1 g, 0.43 mmol) in N-methyl 2-pyrolidone (0.5 mL) was added powdered potassium hydroxide (0.096 g, 1.72 mmol) and allowed to stir for 10 min at RT. 2-trifluoromethyl-5-vinyl pyridine (0.19 g, 1.1 mmol) was added and stirred for further at 35 deg C. for 3 h. Reaction mixture was diluted with brine (5 mL) and extracted with ethyl acetate (3×50 mL). The organic layer was dried over anhydrous sodium sulphate and concentrated under reduced pressure. The crude was purified through column chromatography (5% MeOH:DCM in silica 100-200 mesh, Diameter of column—2.5 cm, Height of silica—approx. 5 inch) to provide the desired compound as brown oil (0.17 g, 45% yield). Isopropyl-2-methyl-5-[2-(6-trifluoromethyl-pyridin-3-yl)-ethyl]-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (0.080 g, 0.19 mmol) was dissolved in THF (2.0 mL). A solution of oxalic acid dihydrate (0.017 g, 0.19 mmol) in THF (2 mL) was added and stirred for 30 min at RT, Precipitate obtained was filtered and dried to give oxalate salt as white solid (0.045 g, 46% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09096591B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-b045de6f10a34b20a2b2d97dd03cd197
출처 메모uspto-grants-2015_08