참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Iodide | HCID 5238 | — |
| 반응물 | Potassium Hydroxide | HCID 14797 | — |
| 반응물 | 2,4,6-Trimethylbenzyl chloride | HCID 74108 | — |
| 반응물 | 2'-deoxy-5'-O-trityl-5-fluorouridine | HCID 10838704 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 2'-deoxy-5-fluoro-3'-O-(2,4,6-trimethylbenzyl)uridine | HCID 14074408 | 55% |
반응 단계
A 1.66 g quantity of 2,4,6-trimethylbenzyl chloride was added to a solution of 4.00 g of 2'-deoxy-5-fluoro-5'-O-trityluridine, 2.30 g of potassium hydroxide and 1.47 g of sodium iodide in 50 ml of dried dioxane. The mixture was stirred at 60° C. for 3 hours. The solvent was distilled off, and ethylacetate and water were added to the residue. The ethyl acetate layer was washed with water and dried over anhydrous sodium sulfate. The ethyl acetate was distilled off and the residue was dissolved in 50 ml of a 80% solution of acetic acid. The resulting solution was left to stand at 70° C. for 2 hours. The reaction mixture was concentrated and water was added to the concentrate. The mixture was rendered weakly basic with an aqueous solution of sodium hydroxide and washed with ether. The aqueous layer was made weakly acidic with a 6N solution of hydrochloric acid and extracted with ethyl acetate. The ethyl acetate layer was washed with water, dried over anhydrous sodium sulfate and concentrated. Ether was added to the concentrate to deposit solids and the solids were recrystallized from ethanol, giving 1.69 g of the title compound in a yield of 55%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US05155113 |
|---|
| 출처 데이터셋 | uspto-grants-1992_10 |
|---|
| ORD ID | ord-86fca4c3106b42fd8a7c7e95ed88cc2f |
|---|
| 출처 메모 | uspto-grants-1992_10 |
|---|