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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2386175Generated: October 31, 2026

Water → N-(5-(5-formylfuran-2-yl)-4-methylthiazol-2-yl)acetamide

https://huagongshe.com/reaction/2386175

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(5-bromo-4-methyl-1,3-thiazol-2-yl)acetamideHCID 822437—
Reactant5-Formylfuran-2-boronic acidHCID 2734355—
CatalystPalladium ChlorideHCID 24290—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductN-(5-(5-formylfuran-2-yl)-4-methylthiazol-2-yl)acetamideHCID 1453274537.6%

Reaction Steps

To a solution of 3.0 g of N-(5-bromo-4-methylthiazol-2-yl)acetamide in 50 mL of NMP was added 3.0 g of 5-formylfuran-2-ylboronic acid. To the stirred solution was then added 300 mg of 1,1 bis-(diphenylphosphino)-ferrocene) palladium dichloride followed by 10 mL of saturated sodium bicarbonate. The resulting biphasic mixture was irradiated at 150° C. in a microwave for 20 min. The resulting mixture was poured into 200 mL of water and filtered. The filtrate was extracted with ether and the ether layers were combined, dried over sodium sulfate and concentrated. The resulting oil was precipitated with methylene chloride and filtered, yielding 1.2 g of N-(5-(5-formylfuran-2-yl)-4-methylthiazol-2-yl)acetamide as an orange solid which was used without further purification. LC/MS: 251.07 (M+H)/2.18 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268818B2
Source datasetuspto-grants-2012_09
ORD IDord-bd27cf2b1efd4a50a4358e2fa564ac30
Source noteuspto-grants-2012_09