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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31001생성일: 2026년 10월 24일

1,2-Dichloroethane → (S)-N-[(S)-5-(2-Benzyloxy-ethyl)-6-oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl]-2-hydroxy-propionamide

https://huagongshe.com/ko/reaction/31001

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물L-Lactic AcidHCID 107689—
반응물(S)-7-amino-5-(2-benzyloxy-ethyl)-5H,7H-dibenzo[b,d]azepin-6-oneHCID 58972512—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물(S)-N-[(S)-5-(2-Benzyloxy-ethyl)-6-oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl]-2-hydroxy-propionamideHCID 58972488—

반응 조건

온도0 °C

반응 단계

(S)-7-Amino-5-(2-benzyloxy-ethyl)-5H,7H-dibenzo[b,d]azepin-6-one (50 mg, 0.14 mmol) and L-(+)-lactic acid (14 mg, 0.15 mmol) were dissolved in THF (2 ml), cooled to 0° C. and under exclusion of moisture subsequently treated with 1-hydroxybenzotriazole (21 mg, 0.15 mmol), EDC (33 mg, 0.17 mmol) and N-diisopropyl-ethylamine (0.05 ml, 0.28 mmol). After stirring for 30 min. at 0° C. and 3 h at ambient temperature, the mixture was diluted with water and ethyl acetate (10 ml each), the phases separated and the organic layer extracted with water, 1N aqueous HCl and saturated aqueous NaCl. After drying over magnesium sulphate and evaporation of the solvent, the title compound was afforded as colourless oil (98%). MS: m/e=431(M−H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425551B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-8da343e23cc24acd828e859b0586d42e
출처 메모uspto-grants-2008_09