돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 509708생성일: 2026년 10월 25일

Triethylamine → 5-(2-fluorophenethyl)-2,3,4,5-tetrahydro-8-iodo-2-methyl-1H-pyrido[4,3-b]indole

https://huagongshe.com/reaction/509708

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물TrifluoroacetateHCID 84468—
반응물2-Fluorophenethyl bromideHCID 2756964—
반응물4-Iodophenylhydrazine hydrochlorideHCID 12208795—
반응물1-Methylpiperidin-4-one hydrochlorideHCID 12210057—
용매EthanolHCID 702—
생성물5-(2-fluorophenethyl)-2,3,4,5-tetrahydro-8-iodo-2-methyl-1H-pyrido[4,3-b]indoleHCID 578762460.5%

반응 단계

Preparation of the title compound was carried out according to General Method 8. 4-Iodophenylhydrazine hydrochloride (500 mg, 2.1 mmol), 2-fluorophenethylbromide (0.3 ml, 2.1 mmol), triethyl amine (0.8 ml, 6.3 mmol) and N-methyl-4-piperidone hydrochloride (312 mg, 2.1 mmol) were taken in ethanol (10 ml) to obtain 5 mg of 5-(2-fluorophenethyl)-2,3,4,5-tetrahydro-8-iodo-2-methyl-1H-pyrido[4,3-b]indole as a trifluoroacetate salt after purification by reverse-phase chromatography (C-18, 500 mm×50 mm, Mobile Phase A=0.05% TFA in water, B=0.05% TFA in acetonitrile, Gradient: 10% B to 80% B in 30 min, injection vol. 5 mL).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09096591B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-521570ed17164ebaa0afba6f902f1fbf
출처 메모uspto-grants-2015_08