Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1788568생성일: 2026년 10월 26일
Sodium Hydroxide → 1-Cyclohexyl-2-(4-oxo-2-phenyl-4H-chromen-6-yl)-1H-benzoimidazole-5-carboxylic Acid
https://huagongshe.com/reaction/1788568
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Hydroxide | HCID 14798 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 4-Oxo-2-phenyl-4H-chromene-6-carboxylic acid | HCID 493377 | — |
| 반응물 | Ferrostatin-1 | HCID 4068248 | — |
| 반응물 | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-Cyclohexyl-2-(4-oxo-2-phenyl-4H-chromen-6-yl)-1H-benzoimidazole-5-carboxylic Acid | HCID 11476797 | — |
반응 단계
4-Oxo-2-phenyl-4H-chromene-6-carboxylic acid (280 mg, 1.05 mmol) was dissolved in DMF (5 mL), and HATU (418 mg, 1.1 eq.) and diisopropyl ethylamine (402 μL) were added. After stirring at room temperature for 15 minutes, 3-amino-4-cyclohexylamino-benzoic acid ethyl ester (303 mg, 1.1 eq.) dissolved in 2 mL DMF was added. After stirring overnight, the reaction was evaporated, dissolved in ethyl acetate and washed with water and brine, dried with sodium sulfate, evaporated and dried overnight. The product was then refluxed in acetic acid for 4h, evaporated to dryness, and coevaporated 2 more times with toluene. Saponification proceeds by dissolving the residue in ethanol (10 mL), adding 10 eq. of 1N NaOH solution and stirring at 40° C. for 4 hr. The ethanol was evaporated, water was added and acidified. The resulting precipitate was purified via reverse-phase HPLC. Yield: 58 mg
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07511145B2 |
|---|
| 출처 데이터셋 | uspto-grants-2009_03 |
|---|
| ORD ID | ord-879bf9131e944162837b5e78db54c54a |
|---|
| 출처 메모 | uspto-grants-2009_03 |
|---|