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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 130741생성일: 2026년 10월 26일

Sodium borohydride → 6-{4-[(2-Cyclopentyl-ethylamino)-methyl]-phenoxy}-nicotinamide

https://huagongshe.com/reaction/130741

반응식

참여 물질

역할이름HCID투입량
반응물Sodium borohydrideHCID 4311764—
반응물2-CyclopentylethanamineHCID 5305650—
반응물6-(4-Formylphenoxy)pyridine-3-carboxamideHCID 56851422—
용매MethanolHCID 887—
생성물6-{4-[(2-Cyclopentyl-ethylamino)-methyl]-phenoxy}-nicotinamideHCID 5973026152.2%

반응 단계

Combine 6-(4-formyl-phenoxy)-nicotinamide (0.61 g, 2.54 mmol) with 2-Cyclopentyl-ethylamine (0.38 g, 3.3 mmol), 2 g of 3 {acute over (Å)} molecular sieves, and 10 mL of methanol. Stir for 18 h under nitrogen. Add sodium borohydride (0.5 g, 13.2 mmol), and stir for 24 h. Filter through Celite, remove the solvent in vacuo. Partition the residue between water (50 mL) and ethyl acetate (100 mL). Dry the organic phase (sodium sulfate), filter, and concentrate in vacuo. Adsorb on silica, and purify on an ISCO® 100 g system (eluting with 95:5:0.5 to 90:10:1 chloroform/ethanol/ammonium hydroxide) to afford 0.45 g of product. HPLC retention time: 5.93 min (98.7% purity), ESMS (M+): 340.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07381719B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-84f3d6a721274a9d824451f4301ec669
출처 메모uspto-grants-2008_06