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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 395695생성일: 2026년 10월 26일

Pyridine → N1-(4-methoxybenzoyl)-N2-[1-(tert-butoxycarbonyl)piperidin-4-ylmethoxycarbonyl]-1,2-benzenediamine

https://huagongshe.com/reaction/395695

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물PhosgeneHCID 6371—
반응물TetrahydrofuranHCID 8028—
반응물N-(2-Aminophenyl)-4-methoxybenzamideHCID 785232—
반응물Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 2764081—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물N1-(4-methoxybenzoyl)-N2-[1-(tert-butoxycarbonyl)piperidin-4-ylmethoxycarbonyl]-1,2-benzenediamineHCID 8658575393%

반응 단계

A solution of 1.9 M phosgene in toluene (2.0 mL) was treated with 1-(tert-butoxycarbonyl)-4-hydroxymethylpiperidine (200 mg, 0.930 mmol). After 1 h, the mixture was concentrated in vacuo and the residue dried under high vacuum for 4 h. The residue was dissolved in methylene chloride (2.5 mL) and then added dropwise to a solution of N1-(4-methoxybenzoyl)-1,2-benzenediamine (230 mg, 0.950 mmol) and pyridine (0.4 mL) in methylene chloride (5 mL) and tetrahydrofuran (1 mL). After 16 h, the mixture was poured into a mixture of water and ethyl acetate. The organic layer was washed once with 1.0 N aqueous hydrochloric acid, once with saturated sodium chloride solution, dried (potassium carbonate), and filtered. Concentration and purification of the residue by flash chromatography (silica gel, ethyl acetate/hexanes) yielded 416 mg (93%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06605626B2
출처 데이터셋uspto-grants-2003_08
ORD IDord-0754f222815940268f72032513eeb72b
출처 메모uspto-grants-2003_08