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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70866생성일: 2026년 10월 24일

3-Aminopropionitrile → (R)-4-biphenyl-4-yl-3-[3-(2-cyano-ethylcarbamoyl)-propionylamino]-butyric acid ethyl ester

https://huagongshe.com/ko/reaction/70866

반응식

참여 물질

역할이름HCID투입량
반응물3-AminopropionitrileHCID 1647—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물(R)-4-biphenyl-4-yl-3-(3-carboxy-propionylamino)-butyric acid ethyl esterHCID 49822223—
용매TetrahydrofuranHCID 8028—
생성물(R)-4-biphenyl-4-yl-3-[3-(2-cyano-ethylcarbamoyl)-propionylamino]-butyric acid ethyl esterHCID 6720876596%

반응 단계

Next, to a solution of (R)-4-biphenyl-4-yl-3-(3-carboxy-propionylamino)-butyric acid ethyl ester (200 mg, 0.522 mmol) in THF (10 mL) at room temperature is added EDC HCl (120 mg, 0.626 mmol) and HOBT (96 mg, 0.626 mmol). The reaction is stirred at room temperature for 10 minutes then added 3-aminopropionitrile (0.046 ml, 0.626 mmol) and TEA (0.087 ml, 0.626 mmol). After 1 hour, 0.5 equivalent of EDC HCl, HOBT, and 3-aminopropionitrile are added and stirred for 16 hours. The reaction mixture is quenched by brine and is extracted with ethylacetate. The combined organic layer is washed with brine and dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The obtained residue is purified by flash chromatography (silica gel, 2% to 5% EtOH/DCM) to give (R)-4-biphenyl-4-yl-3-[3-(2-cyano-ethylcarbamoyl)-propionylamino]-butyric acid ethyl ester (218 mg, 96% yield). HPLC retention time=0.77 minutes (condition E); MS=436 (m+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822534B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-2d4d108ae8a44645926ed110e1bb7ffd
출처 메모uspto-grants-2014_09