Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2252722생성일: 2026년 10월 27일
Citric Acid → Ethanesulfonic acid {6-[2-(5-bromo-pyrimidin-2-yloxy)-ethoxy]-5-p-tolyl-pyrimidin-4-yl}-amide
https://huagongshe.com/reaction/2252722
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Citric Acid | HCID 311 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 5-Bromo-2-chloropyrimidine | HCID 606665 | — |
| 반응물 | Ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-p-tolyl-pyrimidin-4-yl]-amide | HCID 59645277 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Ethanesulfonic acid {6-[2-(5-bromo-pyrimidin-2-yloxy)-ethoxy]-5-p-tolyl-pyrimidin-4-yl}-amide | HCID 10311226 | 34.4% |
반응 단계
Ethanesulfonic acid [6-(2-hydroxy-ethoxy)-5-p-tolyl-pyrimidin-4-yl]-amide (135 mg) was dissolved in THF (15 ml) and sodium hydride (80 mg) was added followed by stirring for 15 min at 50° C. Then 2-chloro-5-bromo-pyrimidine (162 mg) was added and stirring was continued for 8 h at 70 C. The reaction mixture was poured onto ice water, acidified with solid citric acid and extracted with ethylacetate. The combined organic extracts were dried over magnesium sulfate and the solvent was evaporated. The crude material was purified by plate chromatography with ethyl acetate/hexane=½ to give ethanesulfonic acid {6-[2-(5-bromo-pyrimidin-2-yloxy)-ethoxy]-5-p-tolyl-pyrimidin-4-yl}-amide (68 mg) as a white powder. LC-MS: tR: 4.64, [M+H]+: 496.19.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07323465B2 |
|---|
| 출처 데이터셋 | uspto-grants-2008_01 |
|---|
| ORD ID | ord-655d6fd4792649d384053cec1d355535 |
|---|
| 출처 메모 | uspto-grants-2008_01 |
|---|