참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzene | HCID 241 | — |
| 반응물 | Chlorotrimethylsilane | HCID 6397 | — |
| 반응물 | 5-Propyluracil | HCID 73269 | — |
| 반응물 | 3,5-di-(p-chlorobenzoyl)-2-desoxy-D-ribofuranosyl chloride | HCID 22816183 | — |
| 촉매 | Mercuric acetate | HCID 15337 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 5-Propyl-2'-deoxyuridine | HCID 160155 | 166.5% |
반응 단계
To a solution of 15,4 g 5-propyluracil (0.1 mole) and 21,7 g trimethylsilyl chloride (0,2 mole) in 250 ml anhydrous benzene 20.2 g dry triethylamine (0,2 mole) are added dropwise under stirring and exclusion of humidity within a time span of 15 minutes. After further stirring for about 12 hours the unreacted 5-propyl-uracil and the precipitated dry ethylamine hydrochloride are separated and the filtrate is concentrated under vacuum. The residue is dissolved in 150 ml of absolute toluene and under stirring a solution of 43 g 3,5-di-(p-chlorobenzoyl)-2-desoxy-D-ribofuranosyl chloride (0,1 mole) in 500 ml toluene and thereafter 31,8 g mercury (II)-acetate are added and the stirring is continued another 24 hours. After filtration the filtrate is extracted with a 30% aqueous potassium iodide solution and thereafter washed with water. After drying over sodium sulfate the toluene solution is concentrated to approximately 100 ml. Upon standing the protected nucleoside crystallizes. 45 g of a product with melting point 140°-165° C. are obtained.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04271153 |
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| 출처 데이터셋 | uspto-grants-1981_06 |
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| ORD ID | ord-7f07142bd86f4d97b4ba043dbf53adaf |
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| 출처 메모 | uspto-grants-1981_06 |
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