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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 249624생성일: 2026년 10월 26일

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 3-[2-(3-Benzyloxycarbonylamino-propionylamino)-3-(2-ethoxycarbonyl-ethoxy)-2-(2-ethoxycarbonylethoxymethyl)-propoxy]-propionic acid ethyl ester

https://huagongshe.com/reaction/249624

반응식

참여 물질

역할이름HCID투입량
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물N-Benzyloxycarbonyl-beta-alanineHCID 75313—
반응물3-[2-Amino-3-(2-ethoxycarbonyl-ethoxy)-2-(2-ethoxycarbonyl-ethoxymethyl)-propoxy]-propionic acid ethyl esterHCID 11732574—
용매DichloromethaneHCID 6344—
생성물3-[2-(3-Benzyloxycarbonylamino-propionylamino)-3-(2-ethoxycarbonyl-ethoxy)-2-(2-ethoxycarbonylethoxymethyl)-propoxy]-propionic acid ethyl esterHCID 6929661290.1%

반응 단계

The compound 23 was prepared using General Procedure B with amine 1 (4.0 g, 9.49 mmol), N-Cbz-β-alanine (2.54 g, 11.39 mmol), 1-hydrobenzotriazole (HOBt) (1.53 g, 11.39 mmol), and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) (2.18 g, 11.39 mmol) in CH2Cl2 (50 mL). Purification by flash column chromatography (on silica gel, EtOAc:n-hexane=1:3) afforded 5.36 g (90%) of the desired product 23 as a colorless syrup. 1H NMR (CDCl3): δ 7.31 (m, 5H, ArH), 6.16 (s, 1H, NH), 5.66 (s, 1H, NH), 5.08 (s, 2H, OCH2Ar), 4.12 (q, J=6.4 Hz, 6H, OCH2), 3.67 (m, 12H, CH2O), 3.45 (dt, J=7.4, 15.0 Hz, 2H, CH2NHCO), 2.51 (t, J=8.4 Hz, 6H, CH2CO), 2.37 (dt, J=7.4, 8.6 Hz, 2H CH2CO), 1.24 (t, J=6.4 Hz, 9H, CH3).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07862807B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-53737a31a5b7431ca8b92aa627d4b0ca
출처 메모uspto-grants-2011_01