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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1163909생성일: 2026년 10월 24일

N-Ethyltryptamine → N-ethyl-N-(N-benzyloxycarbonylglycyl)-tryptamine

https://huagongshe.com/ko/reaction/1163909

반응식

참여 물질

역할이름HCID투입량
반응물N-EthyltryptamineHCID 6092—
반응물TriethylamineHCID 8471—
반응물BenzyloxycarbonylglycineHCID 14349—
반응물Isobutyl chloroformateHCID 62365—
용매TetrahydrofuranHCID 8028—
생성물N-ethyl-N-(N-benzyloxycarbonylglycyl)-tryptamineHCID 20513176101.6%

반응 조건

온도-15 °C

반응 단계

30 ml of anhydrous tetrahydrofuran and 1.05 g of triethylamine are added to 2.17 g of N-benzyloxycarbonyl-glycine, and 1.43 g of isobutyl chloroformate are added dropwise thereto at -15° C. under stirring. A solution of 1.96 g of N-ethyl-tryptamin (i.e., 3-(2-ethylamino)ethylindole) in 40 ml of anhydrous tetrahydrofuran is added dropwise to the mixture at the same temperature, and said mixture is stirred at 0° C. for one hour and further stirred at room temperature for 16 hours. After the reaction, the reaction mixture is evaporated to remove solvent. The residue (oil) is purified by silica gel chromatography (Solvent: ethyl acetate-chloroform (1:1). 4.0 g of N-ethyl-N-(N-benzyloxycarbonylglycyl)-tryptamine are thereby obtained as a colorless oil. Yield: 100%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04367230
출처 데이터셋uspto-grants-1983_01
ORD IDord-c07ad14976464c3099faf93d61d2dd8f
출처 메모uspto-grants-1983_01