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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231166Generated: October 27, 2026

Acetic Anhydride → 1-Acetoxymethyl-2-(4-methoxy-2-picolylmercapto)-1H-thieno[3,4-d]imidazole

https://huagongshe.com/reaction/231166

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant1-Hydroxymethyl-2-(4-methoxy-2-picolylmercapto)1H-thieno[3,4-d]imidazoleHCID 14154331—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
Product1-Acetoxymethyl-2-(4-methoxy-2-picolylmercapto)-1H-thieno[3,4-d]imidazoleHCID 14154332—

Reaction Steps

1.3 g (4.2 mmol) of the title compound from Example 28 were dissolved in 25 ml of anhydrous pyridine, and 50 mg of 4-dimethylaminopyridine were added. Under a nitrogen atmosphere and while stirring, 6.3 ml acetic anhydride were added dropwise, and the mixture was stirred at room temperature for one hour. It was then poured onto ice water, extracted with methylene chloride, and the organic phase was dried over MgSO4 and concentrated in vacuo. The crystalline solid was recrystallized from ethanol. Melting point 111°-113° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04845118
Source datasetuspto-grants-1989_07
ORD IDord-78a64d4ef68b4ee0999c8357f465b6ba
Source noteuspto-grants-1989_07