Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Idoxuridine | HCID 5905 | — |
| Reactant | p-(Chlorodiphenylmethyl)anisole | HCID 84462 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 18667132 | HCID 18667132 | — |
Reaction Steps
2 g of 5-iodo-2′-deoxyuridine (5.65 mmole) was dissolved in 30 ml of pyridine, 5 ml of TEA and 2.16 g of MMTr-Cl (6.99 mmole) were sequentially added thereto, and stirred at room temperature for 4 hours. Then, pyridine was removed under a reduced pressure with a rotary evaporator, the residue was treated with a mixture of water and CH2Cl2, the CH2Cl2 layer was separated, dried under MgSO4, and then, CH2Cl2 was removed under a reduced pressure. The resulting residue was subjected to column chromatography (silica gel 60, 230˜400 meshes, Merck) to obtain the title compound as a pale yellow solid. The chromatography was conducted using a mixture of CH2Cl2 and methanol as an eluting solution whose mix ratio was gradually changed from 100:1 to 50:1 (v/v).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06884882B1 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-b736c9fb92144566a09a0ae4e567ec10 |
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| Source note | uspto-grants-2005_04 |
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