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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 131001생성일: 2026년 10월 25일

3-Isopropoxypropylamine → 5-{2-Fluoro-4-[(3-isopropoxypropylamino)methyl]phenoxy}pyrazine-2-carboxamide

https://huagongshe.com/reaction/131001

반응식

참여 물질

역할이름HCID투입량
반응물3-IsopropoxypropylamineHCID 76194—
반응물Sodium borohydrideHCID 4311764—
반응물5-(2-Fluoro-4-formylphenoxy)pyrazine-2-carboxamideHCID 59730013—
용매MethanolHCID 887—
생성물5-{2-Fluoro-4-[(3-isopropoxypropylamino)methyl]phenoxy}pyrazine-2-carboxamideHCID 5972990771.2%

반응 단계

Place 5-(2-fluoro-4-formylphenoxy)pyrazine-2-carboxamide (Example 737, Part E) (0.400 g, 1.53 mmol), 3-isopropoxypropylamine (0.197 g, 1.68 mmol) and 3 {acute over (Å)} molecular sieves in a vial. Add methanol (7.7 mL), cap and stir overnight. Add NaBH4 (0.058 g, 1.53 mmol) and stir until the gasses stop evolving. Load the reaction mixture directly onto a 25 g ISCO® pre-load column. Dry the column in a vacuum oven at room temperature. Purify by eluting through a 40 g ISCO® column with 0% to 30% (2.0 M NH3 in methanol) in 80% (ethyl acetate in hexanes). Concentrate the fractions containing the product. Take the solid up in dichloromethane (100 mL) and wash with 1.0 N NaOH (2×25 mL) to give the title compound (0.395 g, 71%): TOF MS ES+ 363.2 (M+H)+, HRMS calcd for C18H24N4O3F 363.1832 (M+H)+, found 363.1821, time 0.57 min; HPLC [YMC-Pro pack C-18 (150×4.6 mm, S-5 microm), 0.05% TFA/acetonitrile in 0.05% TFA/water at 1.0 mL/min, 10-20% over 5 min, 20-95% over 18], tR=9.8 min, 100% purity.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07381719B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-0f5860c2ebe74739b0cbd582b078bfc2
출처 메모uspto-grants-2008_06