Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1848830생성일: 2026년 10월 25일
Triethylamine → (Z)-tert-butyl 5-(benzyloxy)-3-(3-morpholino-3-oxoprop-1-enyl)-1H-indole-1-carboxylate
https://huagongshe.com/reaction/1848830
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Tri-o-tolylphosphine | HCID 80271 | — |
| 반응물 | Acryloylmorpholine | HCID 98723 | — |
| 반응물 | 5-(Benzyloxy)-3-bromo-1H-indole, N-BOC protected | HCID 40428554 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 용매 | Ammonium Chloride | HCID 25517 | — |
| 생성물 | (Z)-tert-butyl 5-(benzyloxy)-3-(3-morpholino-3-oxoprop-1-enyl)-1H-indole-1-carboxylate | HCID 67227351 | — |
반응 단계
A mixture of tert-butyl 5-(benzyloxy)-3-bromo-1H-indole-1-carboxylate (2.011 g), 1-morpholinoprop-2-en-1-one (0.776 g), palladium acetate (31 mg), tri-o-tolylphosphine (187 mg) and triethylamine (1.14 mL) in N,N-dimethylformamide (14 mL) under nitrogen atmosphere was stirred at 100° C. overnight. The mixture was diluted with ethyl acetate and saturated ammonium chloride. The aqueous layer was extracted with ethyl acetate and the combined organic layers were dried over MgSO4, filtered and concentrated. The residue was purified by flash chromatography (80% ethyl acetate-hexane) to give the desired product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08952157B2 |
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| 출처 데이터셋 | uspto-grants-2015_02 |
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| ORD ID | ord-eed66c9767de4fff9e8f32adad20dc0b |
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| 출처 메모 | uspto-grants-2015_02 |
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