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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1741470생성일: 2026년 10월 26일

1,2-Dichloroethane → 3-t-Butoxycarbonylamino-2-(RS)-[(Naphth-2-ylmethyl)-1H-imidazol-5-yl]acetylamino-propionic acid methyl ester

https://huagongshe.com/reaction/1741470

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물TriethylamineHCID 8471—
반응물3-hydroxy-1,2,3-benzotriazin-4(3H)-oneHCID 73026—
반응물Methyl 2-amino-3-[(2-methylpropan-2-yl)oxycarbonylamino]propanoateHCID 3442239—
반응물1-(2-naphthylmethyl)-1H-imidazol-5-ylacetic acid hydrochlorideHCID 70206205—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물3-t-Butoxycarbonylamino-2-(RS)-[(Naphth-2-ylmethyl)-1H-imidazol-5-yl]acetylamino-propionic acid methyl esterHCID 67571717—

반응 단계

To a solution of 2-[l-(Naphth-2-ylmethyl)-1H-imidazol-5-yl]acetic acid hydrochloride (3.83 g, 12.7 mmol), 3-t-butoxycarbonylamino-2(R,S)- aminopropionic acid methyl ester (3.33 g, 15.3 mmol), HOOBT (2.30 g, 14.1 mmol), and triethylamine (5.80 ml, 42.0 mmol) in DMF (150 ml) at 0° C., was added EDC (2.67 g, 13.9 mmol). The reaction was stirred at room temperature for 18 hrs, diluted with EtOAc and the organic layer washed with sat. aq NaHCO3, brine, dried (Na2SO4), and the solvent evaporated in vacuo. The residue was chromatographed (SiO2, 5% MeOH in CH2Cl2) to afford the title compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05972984
출처 데이터셋uspto-grants-1999_10
ORD IDord-1719258bfaf7426085c3f2ab912e3158
출처 메모uspto-grants-1999_10