Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2297053생성일: 2026년 10월 26일
2,3,5,6-Tetrafluorophenol → N-(1-methyl-3-isobutyl-indole-2-cabonyl)-valinyl-3-amino-4-oxo-5-(2,3,5,6-tetrafluorophenyloxy)-pentanoic acid, tert-butyl ester
https://huagongshe.com/reaction/2297053
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,3,5,6-Tetrafluorophenol | HCID 69858 | — |
| 반응물 | Potassium Fluoride | HCID 522689 | — |
| 반응물 | N-[(1-methyl-3-isobutyl-indole-2-cabonyl)valinyl]-3-amino-5-bromo-4-oxo-pentanoic acid, tert-butyl ester | HCID 86756359 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | N-[(1-methyl-3-isobutyl-indole-2-cabonyl)valinyl]-3-amino-4-oxo-5-(2,3,5,6-tetrafluorophenyloxy)-pentanoic acid, tert-butyl Ester | HCID 86756358 | — |
| 생성물 | N-(1-methyl-3-isobutyl-indole-2-cabonyl)-valinyl-3-amino-4-oxo-5-(2,3,5,6-tetrafluorophenyloxy)-pentanoic acid, tert-butyl ester | HCID 131723666 | 44% |
반응 단계
Potassium fluoride (21.6 mg, 0.37 mmol) was added to a solution of N-[(1-methyl-3-isobutyl-indole-2-cabonyl)valinyl]-3-amino-5-bromo-4-oxo-pentanoic acid, tert-butyl ester (86.1 mg, 0.149 mmol) and 2,3,5, 6-tetrafluorophenol (27.0 mg, 0.163 mmol in DMF (2.0 ml). After stirring at room temperature for 3 hours, the reaction mixture was partitioned between ethyl acetate and water. The aqueous layer was back-extracted with ethyl acetate. The organic layers were combined, washed with saturated NaHCO3 solution, and brine, dried over sodium sulfate, and concentrated. The residue was triturated with ether to give the titled product, N-(1-methyl-3-isobutyl-indole-2-cabonyl)-valinyl-3-amino-4-oxo-5-(2,3,5,6-tetrafluorophenyloxy)-pentanoic acid, tert-butyl ester as a white solid (43.8 mg, 44%). TLC (hexane/EtOAc, 50/50): Rf=0.50.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06489353B2 |
|---|
| 출처 데이터셋 | uspto-grants-2002_12 |
|---|
| ORD ID | ord-b8a4c2d1154744018ded014a58ca1e72 |
|---|
| 출처 메모 | uspto-grants-2002_12 |
|---|