참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-Ethyltryptamine | HCID 6092 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Benzyloxycarbonylglycine | HCID 14349 | — |
| 반응물 | Isobutyl chloroformate | HCID 62365 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | N-ethyl-N-(N-benzyloxycarbonylglycyl)-tryptamine | HCID 20513176 | 101.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04367230 |
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| 출처 데이터셋 | uspto-grants-1983_01 |
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| ORD ID | ord-c07ad14976464c3099faf93d61d2dd8f |
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| 출처 메모 | uspto-grants-1983_01 |
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