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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 501072생성일: 2026년 10월 24일

1,1'-Carbonyldiimidazole → 2-oxo-3-(1-benzylpiperidin-4-yl)-2,3-dihydro-1H-imidazo[4,5-c]pyridine

https://huagongshe.com/ko/reaction/501072

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물4-Amino-3-[(1-benzylpiperidin-4-yl)amino)pyridineHCID 22293245—
용매TetrahydrofuranHCID 8028—
생성물2-oxo-3-(1-benzylpiperidin-4-yl)-2,3-dihydro-1H-imidazo[4,5-c]pyridineHCID 2229317091.7%

반응 단계

A solution of 4-amino-3-[(1-benzylpiperidin-4-yl)amino)pyridine (2.8 g, 9.9 mmol) and carbonyldiimidazole (3.0 g, 18.5 mmol) in tetrahydrofuran (100 mL) was refluxed overnight. The reaction was cooled, concentrated and partitioned between chloroform (500 mL) and saturated sodium carbonate (100 mL). The organic phase was dried over magnesium sulfate and concentrated to give the title compound (2.8 g). MS 209 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772224B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-e3674d3b283344e7a903aedef57e431b
출처 메모uspto-grants-2010_08