Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1379050생성일: 2026년 10월 26일
Ethyl Acetate → 2-[(2-bromo)acetyl]amino-3-(1H-indol-3-yl)1-[N-(2-methoxybenzyl)acetylamino]propane
https://huagongshe.com/reaction/1379050
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Bromoacetyl bromide | HCID 61147 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 2-amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propane | HCID 22508955 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-[(2-bromo)acetyl]amino-3-(1H-indol-3-yl)1-[N-(2-methoxybenzyl)acetylamino]propane | HCID 69736949 | — |
반응 단계
To a stirring solution of 2-amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propane (7.51 g, 21.369 mmoles) in anhydrous tetrahydrofuran (100 ml) under a nitrogen atmosphere at 0° C. was added diisopropylethylamine (4.1 ml, 23.537 mmoles) and bromoacetyl bromide (2.05 ml, 23.530 mmoles). After 2 hours, ethyl acetate was added and the reaction mixture washed with water twice, 1.0N hydrochloric acid (2×), saturated sodium bicarbonate solution (2×), and brine. The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated to a tan foam on a rotary evaporator. In this manner the 2-[(2-bromo)acetyl]amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propane was obtained in quantitative yield. No further purification was necessary.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05670499 |
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| 출처 데이터셋 | uspto-grants-1997_09 |
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| ORD ID | ord-808277e1f054413d966db4e1c92d4e86 |
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| 출처 메모 | uspto-grants-1997_09 |
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