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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482963Generated: October 30, 2026

Imidazole → N-(4-(((tert-butyldiphenylsilyl)oxy)methyl)-2-iodo-5-(methylthio)phenyl)methanesulfonamide

https://huagongshe.com/reaction/1482963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-ButyldiphenylchlorosilaneHCID 94078—
ReactantN-(4-(hydroxymethyl)-2-iodo-5-(methylthio)phenyl)methanesulfonamideHCID 89814728—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductN-(4-(((tert-butyldiphenylsilyl)oxy)methyl)-2-iodo-5-(methylthio)phenyl)methanesulfonamideHCID 89814652—

Reaction Steps

To a stirred solution of N-(4-(hydroxymethyl)-2-iodo-5-(methylthio)phenyl)methanesulfonamide (6.4 g, 17.2 mmol) and imidazole (1.76 g, 25.8 mmol) in CH2Cl2 (100 mL) and DMF (50 mL) at 0° C. was added tert-butyldiphenylsilyl chloride (5.8 mL, 22.4 mmol). The mixture was allowed to stir at rt overnight. The mixture was diluted with CH2Cl2 (100 mL), washed with 1N HCl solution, sat. aq. NaHCO3 and brine, dried over anhydrous Na2SO4, filtered and concentrated in vacuo to afford N-(4-(((tert-butyldiphenylsilyl)oxy)methyl)-2-iodo-5-(methylthio)phenyl)methanesulfonamide. It was used for next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09416135B2
Source datasetuspto-grants-2016_08
ORD IDord-6c81464cf0a544ad907a62c65b27020c
Source noteuspto-grants-2016_08