Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Methanethiol → 2'-Deoxy-2'-methylthio-5-methyluridine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Methanethiol | HCID 878 | — |
| 반응물 | 1,1,3,3-Tetramethylguanidine | HCID 66460 | — |
| 반응물 | 2,2'-Anhydro-1-beta-arabinofuranosylthymine | HCID 168045 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2'-Deoxy-2'-methylthio-5-methyluridine | HCID 10334293 | 74.1% |
반응 단계
2,2′-Anhydro-5-methyluridine (17.02 g, 70.6 mmol), methanethiol (16.3 g, 339 mmol), 1,1,3,3-tetramethylguanidine (40.6 g, 353 mmol) and DMF (150 mL) were heated at 60° C. After 12 hours, the products were cooled and concentrated under reduced pressure. The residual oil was purified by short silica gel column chromatography (300 g). Pooling and concentrating appropriate fractions, which were eluted with CH2Cl2—MeOH (93:7), furnished the title compound as a white foam (15.08 g, 74.1%), which was crystallized from EtOH—CH2Cl2 as white needles.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07138517B2 |
| 출처 데이터셋 | uspto-grants-2006_11 |
| ORD ID | ord-93e2a9d0dda34df689dc139f3bb2a8c9 |
| 출처 메모 | uspto-grants-2006_11 |