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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 251070생성일: 2026년 10월 26일

Potassium Carbonate → {4-[(3-Fluoro-pyridin-2-ylmethyl)-amino]-butyl}-methyl-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/251070

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Sodium BicarbonateHCID 516892—
반응물N-(4-Aminobutyl)-N-methyl carbamic acid tert-butyl esterHCID 2756377—
반응물Sodium borohydrideHCID 4311764—
반응물3-Fluoro-2-pyridinecarboxaldehydeHCID 11344017—
용매MethanolHCID 887—
생성물{4-[(3-Fluoro-pyridin-2-ylmethyl)-amino]-butyl}-methyl-carbamic acid tert-butyl esterHCID 6727186174%

반응 단계

A mixture of (4-amino-butyl)-methyl-carbamic acid tert-butyl ester (0.202 g, 1.00 mmol), 3-fluoro-pyridine-2-carbaldehyde (0.125 g, 1.00 mmol) and K2CO3 (0.138 g, 1.00) in MeOH (5 mL) was stirred for 16 h. The mixture was filtered through a celite cake and NaBH4 (0.050 g, 1.3 mmol) was added to the filtrate, and the mixture was stirred for 30 min. Saturated aqueous NaHCO3 (20 mL) was added, and MeOH was removed. The aqueous residue was extracted with CH2Cl2 (3×30 mL). The organic extracts were combined and dried over anhydrous Na2SO4. After filtration the solvent was removed by evaporation under vacuum, and the residue was purified by flash chromatography on a silica gel column (50:2:1 CH2Cl2/MeOH/NH4OH), affording {4-[(3-fluoro-pyridin-2-ylmethyl)-amino]-butyl}-methyl-carbamic acid tert-butyl ester as a colorless oil (0.230 g, 74%). 1H NMR (CDCl3) δ 1.42 (s, 9H), 1.48-1.54 (m, 4H), 2.61-2.68 (m, 2H), 2.80 (s, 3H), 3.14-3.22 (m, 2H), 3.96 (s, 2H), 7.11-7.20 (m, 1H), 7.30-7.36 (m, 1H), 8.33-8.38 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863293B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-c56fed248a64434cb85fd83a053f079e
출처 메모uspto-grants-2011_01