Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1,8-Diazabicyclo(5.4.0)undec-7-ene → [5-(4-Fluorophenylcarbamoyl)pyrimidin-2-yloxy]acetic acid benzyl ester
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| 반응물 | Benzyl 2-hydroxyacetate | HCID 561337 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 반응물 | 2-Methanesulfinylpyrimidine-5-carboxylic acid (4-fluorophenyl)amide | HCID 86760384 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 용매 | Ethyl acetate hexane | HCID 21226206 | — |
| 생성물 | [5-(4-Fluorophenylcarbamoyl)pyrimidin-2-yloxy]acetic acid benzyl ester | HCID 16004800 | 30.2% |
반응 단계
To a solution of 2-methanesulfinylpyrimidine-5-carboxylic acid (4-fluorophenyl)amide (173 mg, contaminated with 10% sulfone, 0.62 mmol) in THF (6 mL) was added benzyl glycolate (128 μL, 0.90 mmol) followed by potassium tert-butoxide (1 M in THF, 0.3 mL, 0.3 mmol) and DBU (139 μL, 0.93 mmol). The solution was stirred for 5 h, diluted with 50% ethyl acetate/hexane, and passed through a plug of SiO2 followed by washing with 40% ethyl acetate/hexane. The filtrate was concentrated in vacuo, and the residue flash-chromatographed on SiO2 with 35% ethyl acetate/hexane to afford 71.5 mg (30% yield) of the titled product as a white solid. ESI-MS m/z 382 (MH+), 380 (M−H)−.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07176310B1 |
| 출처 데이터셋 | uspto-grants-2007_02 |
| ORD ID | ord-7ec0e26be06e4a9b84a8b8362dc49978 |
| 출처 메모 | uspto-grants-2007_02 |