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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816511Generated: November 2, 2026

Idoxuridine → HCID 18667132, compound

https://huagongshe.com/reaction/1816511

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIdoxuridineHCID 5905—
Reactantp-(Chlorodiphenylmethyl)anisoleHCID 84462—
SolventPyridineHCID 1049—
ProductHCID 18667132HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884882B1
Source datasetuspto-grants-2005_04
ORD IDord-b736c9fb92144566a09a0ae4e567ec10
Source noteuspto-grants-2005_04