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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2509생성일: 2026년 10월 26일

Tert-butoxycarbonylalanine → 4-[(S)-2-(tert-Butoxycarbonylamino)propionyl]aminomethyl-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(2-methoxyethyl)benzamide

https://huagongshe.com/reaction/2509

반응식

참여 물질

역할이름HCID투입량
반응물Tert-butoxycarbonylalanineHCID 85082—
반응물Sodium BicarbonateHCID 516892—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물4-Aminomethyl-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(2-methoxyethyl)benzamideHCID 19689858—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물4-[(S)-2-(tert-Butoxycarbonylamino)propionyl]aminomethyl-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(2-methoxyethyl)benzamideHCID 6780138872.6%

반응 단계

4-Aminomethyl-N-{2-[4-(4-fluorobenzoyl)piperidino]ethyl}-N-(2-methoxyethyl)benzamide (120 mg, 0.245 mmol) was dissolved in methylene chloride (5 ml) to which were subsequently added Boc-L-alanine (46.4 mg, 0.245 mmol) and EDC hydrochloride (52 mg, 0.270 mmol) while cooling in an ice bath. After 4 hours of stirring at the same temperature, the reaction solution was mixed with water (10 ml), adjusted to pH 8 with saturated sodium bicarbonate aqueous solution and then extracted with methylene chloride. Thereafter, the resulting organic layer was dried on anhydrous sodium carbonate, the solvent was removed by evaporation, and the resulting residue was purified by a silica gel column chromatography (ethyl acetate) to obtain 109 mg (68.9%) of the title compound in a colorless amorphous form.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05728835
출처 데이터셋uspto-grants-1998_03
ORD IDord-455b69c6551746be8a9a9cf6a7695e89
출처 메모uspto-grants-1998_03