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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2223246생성일: 2026년 10월 26일

1,2-Dichloroethane → [2-(3,4-Dihydro-1H-isoquinolin-2-yl)-1-(1H-indol-3-ylmethyl)-2-oxo-ethyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/2223246

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물1,2,3,4-TetrahydroisoquinolineHCID 7046—
반응물DiisopropylethylamineHCID 81531—
반응물N-tert-Butoxycarbonyl-L-tryptophanHCID 83169—
반응물HCID 178418300HCID 178418300—
용매TetrahydrofuranHCID 8028—
생성물[2-(3,4-Dihydro-1H-isoquinolin-2-yl)-1-(1H-indol-3-ylmethyl)-2-oxo-ethyl]-carbamic acid tert-butyl esterHCID 69900649—

반응 단계

tert-Butyloxycarbonyl-L-tryptophan (3.00 g, 9.9 mmol) and 1,2,3,4-tetrahydroisoquinoline (1.31 g, 9.9 mmol) were suspended in THF (20 ml). At a temperature of 0° C., hydroxybenzotriazole (1.33 g, 9.9 mmol), diisopropylethylamine (1.27 g, 9.9 mmol), and EDC (N-3-dimethylaminopropyl-N′-ethylcarbodiimide hydrochloride, 1.89 g, 9.9 mmol) were added. The reaction mixture was stirred overnight at r.t. The solvent was evaporated, the residue was taken up in ethyl acetate, washed with water, and dried (Na2SO4). After evaporation of the solvent, the title compound, MS: m/e=420.5 (M+H+), (2.90 g, 70%) was obtained by chromatographic purification of the residue (silica gel, MeOH, CH2Cl2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07375099B2
출처 데이터셋uspto-grants-2008_05
ORD IDord-3b7b631a0825407d8466ed1fdd2dc211
출처 메모uspto-grants-2008_05