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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 130688생성일: 2026년 10월 26일

Potassium Carbonate → 6-(4-(2-(Benzylamino)ethyl)phenoxy)nicotinamide

https://huagongshe.com/reaction/130688

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물DimethylacetamideHCID 31374—
반응물6-ChloronicotinamideHCID 80456—
반응물4-(2-(Benzylamino)ethyl)phenolHCID 3042572—
용매2,2,4-TrimethylpentaneHCID 10907—
생성물6-(4-(2-(Benzylamino)ethyl)phenoxy)nicotinamideHCID 44434057127.9%

반응 단계

Add 6-chloronicotinamide (7.03 g, 44.90 mmol) to a stirred solution of 4-(2-benzylamino-ethyl)-phenol (10.10 g, 44.43 mmol), potassium carbonate (15.35 g, 111.1 mmol), dimethylacetamide (138 mL), and isooctane (16 mL). Using a Dean-Stark trap, heat the reaction to reflux under nitrogen for 6 h. Cool the reaction mixtures to room temperature, filter off the solids, and concentrate most of the solvent off on a rotary evaporator. Take the residue up in ethyl acetate (200 mL) and add 1N hydrochloric acid (200 mL). Stir for 15 minutes and filter off the precipitate washing with ethyl acetate. Dissolve the solid in 400 mL of boiling 1:1 methanol/water. To this solution add 5N sodium hydroxide (35 mL) and allow the solution to cool to room temperature. Filter and wash with water to yield 19.74 g (83%) of 6-[4-(2-benzylamino-ethyl)-phenoxy]-nicotinamide: mass spectrum (ion spray): m/z=348.1 (M+1); 1H NMR (CDCl3): 8.58 (d, 1H), 8.15 (dd, 1H), 7.34-7.24 (m, 7H), 7.06 (d, 2H), 6.93 (d, 1H), 6.08 (br s, 2H), 3.82 (s, 2H), 2.92 (t, 2H), 2.84 (t, 2H), 1.33 (br s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07381719B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-bc1919c87b5147469d0e181387267f4b
출처 메모uspto-grants-2008_06