Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10286생성일: 2026년 10월 24일
Triethylamine → 4-[3-(tert-Butoxycarbonylamino)pyrrolidin-1-yl]-2,3-difluorobenzoic acid ethyl ester
https://huagongshe.com/ko/reaction/10286
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Benzoic acid, 2,3,4-trifluoro-, ethyl ester | HCID 594559 | — |
| 반응물 | tert-butyl N-(pyrrolidin-3-yl)carbamate | HCID 2757234 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 4-[3-(tert-Butoxycarbonylamino)pyrrolidin-1-yl]-2,3-difluorobenzoic acid ethyl ester | HCID 21041177 | 70.1% |
반응 단계
A solution of 2,3,4-trifluorobenzoic acid ethyl ester (Example 1g, 3.70 g, 18.1 mmol), pyrrolidin-3-ylcarbamic acid tert-butyl ester (4.02 g, 21.6 mmol), and triethylamine (18.0 mL, 129 mmol) in acetonitrile (50 mL) is heated at 50° C. under nitrogen atmosphere for 4.5 hours. The solution is concentrated in vacuo and poured into a saturated NaHCO3 solution. The mixture is then extracted with chloroform, and the combined organic extracts are washed with brine, dried with Na2SO4, filtered, and the mixture concentrated in vacuo. The resulting residue is then purified by column chromatography (1:7 ethyl acetate/hexanes) to afford the title compound (4.70 g). 1H NMR (CDCl3): δ 7.59–7.49 (m, 1H), 6.35–6.26 (m, 1H), 4.88–4.84 (bd, 1H), 4.39–4.28 (m, 3H), 3.81–3.50 (m, 3H), 3.48–3.34 (m, 1H), 2.32–2.15 (m, 1H), 2.02–1.76 (m, 1H), 1.45 (s, 9H), 1.40 (t, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07094780B1 |
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| 출처 데이터셋 | uspto-grants-2006_08 |
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| ORD ID | ord-4cd038f4ec2c4063a2e06a388d2c39ee |
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| 출처 메모 | uspto-grants-2006_08 |
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