Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 929185Generated: November 1, 2026

Ethyl Acetate → 6-chloro-2-(methylsulfonyl)-3-((2-(trimethylsilyl)ethoxy)methyl)-3H-imidazo[4,5-c]pyridine

https://huagongshe.com/reaction/929185

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Chloromethyl 2-(trimethylsilyl)ethyl etherHCID 2724271—
Reactant6-chloro-2-(methylsulfonyl)-3H-imidazo[4,5-c]pyridineHCID 90042073—
SolventDimethylformamideHCID 6228—
Product6-chloro-2-(methylsulfonyl)-3-((2-(trimethylsilyl)ethoxy)methyl)-3H-imidazo[4,5-c]pyridineHCID 90042145—

Reaction Steps

To a stirring solution of 6-chloro-2-(methylsulfonyl)-3H-imidazo[4,5-c]pyridine (847 mg, 3.66 mmol) and N,N-diisopropylethylamine (5.11 mL, 29.20 mmol) in anhydrous DMF (25.0 mL) was added 2-(trimethylsilyl)ethoxymethyl chloride (3.24 mL, 18.28 mmol). The reaction was stirred under N2 at RT for 18 h, then added to EtOAc (1.4 L) and washed with saturated NH4Cl (0.3 L). The aqueous layer was separated and back-extracted with EtOAc (0.3 L). The combined organic layers were evaporated under reduced pressure. Flash chromatography of the resulting residue utilizing a 40 g silica RediSep Rf® Gold column and employing a 0-30% EtOAc/hexane gradient afforded the title compound. LC-MS: calculated for C13H20ClN3O3SSi 361.07 observed m/e: 362.31 (M+H)+ (Rt 1.32/2.0 min)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290517B2
Source datasetuspto-grants-2016_03
ORD IDord-eb3553aff22944769b1a5a93a9f7ebbf
Source noteuspto-grants-2016_03