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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 368875생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/368875

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 번호US06133446
출처 데이터셋uspto-grants-2000_10
ORD IDord-b9ec82874c98434f919c817e0e47cfa8
출처 메모uspto-grants-2000_10