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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 228152생성일: 2026년 10월 24일

2-Methoxybenzaldehyde → 6-{4-[2-(2-Methoxy-benzylamino)-ethyl]-phenoxy}-nicotinamide

https://huagongshe.com/ko/reaction/228152

반응식

참여 물질

역할이름HCID투입량
반응물2-MethoxybenzaldehydeHCID 8658—
반응물Sodium borohydrideHCID 4311764—
반응물6-[4-(2-Amino-ethyl)-phenoxy]-nicotinamideHCID 59730017—
용매MethanolHCID 887—
생성물6-{4-[2-(2-Methoxy-benzylamino)-ethyl]-phenoxy}-nicotinamideHCID 5973039685.4%

반응 단계

Add three-angstrom molecular sieves to a stirred solution of 6-[4-(2-amino-ethyl)-phenoxy]-nicotinamide (0.1000 g, 0.3887 mmol) (compound of example 33), 2-methoxybenzaldehyde (0.047 mL, 0.39 mmol), and methanol (5 mL). Agitate the reaction for 18 h on a platform shaker at room temperature. Add sodium borohydride and agitate for 1 h at room temperature. Filter to remove the molecular sieves and load the reaction mixture directly onto a 10 g prepacked SCX cartridge. Flush with methanol (150 mL) and elute the product off the SCX cartridge with 2 M ammonia in methanol (50 mL). Concentrate on a rotary evaporator to give 0.1253 g (85%) of 6-{4-[2-(2-methoxy-benzylamino)-ethyl]-phenoxy}-nicotinamide: HPLC (30/70 to 90/10 ACN/(0.1% TFA in water) Zorbax SB-Phenyl Column 4.6 mm×15 cm×5 micron: Retention time: 4.14 minutes, Purity: 97.9%; mass spectrum (ion spray): m/z=378.1 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560463B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-b3acef7e9e4a4039970a72a40a2eb3ff
출처 메모uspto-grants-2009_07