참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Iodine chloride | HCID 24640 | — |
| 반응물 | 2',3'-Dideoxyuridine | HCID 65161 | — |
| 용매 | Methanol | HCID 887 | — |
| 생성물 | 5-Iodo-2',3'-dideoxyuridine | HCID 451862 | 66% |
반응 단계
Dideoxyuridine (2.122 g, 10.0 mmol) was dissolved in 30 mL of warm methanol and, after cooling to 25°, iodine monochloride (4.06 g, 25 mmol, 2.5 eq. Fisher) in methanol (20 mL) was added over 5 minutes. The dark purple reaction mixture was heated in a 50° bath under nitrogen for 20 minutes and then immediately cooled in an ice-water bath. After standing without stirring for 165 minutes, the resulting precipitate was collected by filtration and washed with cold methanol (2×10 mL). Vacuum-drying overnight afforded 2.232 g (66%) of iodide 21 as off-white microcrystals. This material was used without further purification in the next reaction, but other preparations were purified by chromatography or recrystallization from boiling methanol (30 mL/g) to give white needles (mp d 160°-164°). NMR indicated that the crude precipitate was homogeneous, but also that the 5'-hydroxy proton was very broad due to exchange catalyzed by trace impurities. Chromatographed or recrystallized materials afforded spectra in which this proton was, as usual, a sharp triplet.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05625081 |
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| 출처 데이터셋 | uspto-grants-1997_04 |
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| ORD ID | ord-5817d2c8e8db465e9c1b92bbfc342f50 |
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| 출처 메모 | uspto-grants-1997_04 |
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