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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1417857생성일: 2026년 10월 26일

1-benzyl-N-methylpiperidin-4-amine → U 99363

https://huagongshe.com/reaction/1417857

반응식

참여 물질

역할이름HCID투입량
반응물1-benzyl-N-methylpiperidin-4-amineHCID 4136128—
반응물2-Bromo-3-ethoxypyridineHCID 10631926—
용매DichloromethaneHCID 6344—
생성물U 99363HCID 133107—

반응 단계

A mixture of N-(1-benzylpiperidin-4-yl)-N-methylamine (XXVII, 4.80 g) and 2-bromo-3-ethoxypyridine (XXVIIIa, 2.3805 g) is placed in a metal, screw cap reaction vessel using dichloromethane as the transfer solvent. Reduced pressure is applied to the vessel with heating at 50° to 60° for 45 min to remove dichloromethane. The vessel is then sealed and heated at 160° to 165° for 2 days. After cooling, the resulting solids are dissolved in dichloromethane and washed with water and saline. The organic phases are dried over magnesium sulfate and concentrated under reduced pressure to give the product, which is chromatographed (silica gel; eluting with ethyl acetate/hexane (30/70) followed by ethyl acetate/hexane (50/50)), to give N-(1-benzylpiperidin-4-yl)-N-(3-ethoxypyridin-2-yl)-methylamine (XXVIII, Chart G); MS (m/z) 325; IR (neat) 1462, 1211, 1481, 1589 and 1450 cm-1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05877317
출처 데이터셋uspto-grants-1999_03
ORD IDord-cc319317b3864991820ceff95256e646
출처 메모uspto-grants-1999_03