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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 11636생성일: 2026년 10월 24일

Methyl 3-aminopropanoate hydrochloride → 3-(5-Chloro-2-{2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-benzylamino)-propionic Acid Methyl Ester

https://huagongshe.com/ko/reaction/11636

반응식

참여 물질

역할이름HCID투입량
반응물Methyl 3-aminopropanoate hydrochlorideHCID 2734767—
반응물Sodium cyanoborohydrideHCID 5003444—
반응물(2R,5S)-5-Chloro-2-{2-[4-(4-fluoro-benzyl)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-benzaldehydeHCID 53673807—
용매Acetic AcidHCID 176—
용매MethanolHCID 887—
용매TriethylamineHCID 8471—
용매Ethyl AcetateHCID 8857—
생성물3-(5-Chloro-2-{2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-benzylamino)-propionic Acid Methyl EsterHCID 6965527038.4%

반응 단계

To a solution of 5-chloro-2-{2-[4-(4-fluoro-benzyl)-(2R,5S)-2,5-dimethyl-piperazin-1-yl]-2-oxo-ethoxy}-benzaldehyde (0.075 g, 0.18 mmol) in methanol (2 mL) was added 3-amino-propionic acid methyl ester hydrochloride salt (0.063 g, 0.45 mmol) and the pH of the solution was adjusted to 5–6 with triethylamine and acetic acid. The reaction mixture was stirred at ambient temperature for 1 hour. To the resulting reaction mixture was added sodium cyanoborohydride (0.023 g, 0.36 mmol), and the pH of the solution was again adjusted to pH 5 with acetic acid and triethylamine. The reaction mixture was stirred at ambient temperature overnight, diluted with ethyl acetate and washed with saturated aqueous sodium hydrogen carbonate. The organic layer was dried over magnesium sulfate, filtered and concentrated in vacuo. The crude product was purified by chromatography on silica gel to give the title compound (0.035 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07098212B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-bc7c522e78254b1bac83549a81ef66f7
출처 메모uspto-grants-2006_08