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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2419325Generated: November 3, 2026

Methyl p-toluenesulfonate → 2-bromo-4-(N-methylacetamido)thiazole

https://huagongshe.com/reaction/2419325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl p-toluenesulfonateHCID 6645—
ReactantSodium hydrideHCID 24758—
Reactant4-Acetamido-2-bromo-thiazoleHCID 20294043—
SolventAcetonitrileHCID 6342—
Product2-bromo-4-(N-methylacetamido)thiazoleHCID 2037716832%

Reaction Steps

A solution of 4-acetamido-2-bromothiazole and methyl tosylate (4.65 g, 25 mM) in dry acetonitrile (125 ml) was treated with a 60% dispersion of sodium hydride in oil (1 g, 25 mM) and the mixture stirred 72 hours at ambient temperature. The reaction mixture was filtered and the filtrate evaporated under reduced pressure. The residue was chromatographed on silica (Woelm grade 1, 150 g) using 2% methanol in chloroform as eluant. Evaporations of the appropriate fractions followed by recrystallisation from hexane gave 2-bromo-4-(N-methylacetamido)thiazole (1.9 g, 32%) mp 84° C. Found: C, 30.55; H, 2.95; N, 11.8%, C6H7N2BrOS requires C, 30.7; H, 3.0; N, 11.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04105773
Source datasetuspto-grants-1978_08
ORD IDord-0e6177a085d14aae9e36264aadc3c510
Source noteuspto-grants-1978_08