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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625667Generated: November 1, 2026

Pyridine → Methyl 4-{[(4'-chloro-4-methylbiphenyl-3-yl)acetyl]amino}-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/625667

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethyl 4-amino-1,3-thiazole-5-carboxylateHCID 15832487—
Reactant(4'-Chloro-4-methylbiphenyl-3-yl)acetyl chlorideHCID 23390525—
SolventAcetonitrileHCID 6342—
ProductMethyl 4-{[(4'-chloro-4-methylbiphenyl-3-yl)acetyl]amino}-1,3-thiazole-5-carboxylateHCID 8982591939.7%

Reaction Steps

1.8 g (11.38 mmol) of methyl 4-amino-1,3-thiazole-5-carboxylate were dissolved in 40 acetonitrile, and 1.8 ml (22.76 mmol) of pyridine were added. After 5 min of stirring at room temperature (RT), a solution of 3.18 g (11.38 mmol) of (4′-chloro-4-methylbiphenyl-3-yl)acetyl chloride (obtained from (4′-chloro-4-methylbiphenyl-3-yl)acetic acid according to WO 99/48869 A1) in 20 ml of acetonitrile was added dropwise. The mixture was stirred at RT for 12 h. The precipitate formed was filtered off, washed with water and dried under reduced pressure. The resulting mother liquor was concentrated by evaporation, dissolved in chloroform and chromatographed (ethyl acetate/n-heptane: 20/80 to 80/20). This gives a total of 1.81 g of methyl 4-{[(4′-chloro-4-methylbiphenyl-3-yl)acetyl]amino}-1,3-thiazole-5-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09307767B2
Source datasetuspto-grants-2016_04
ORD IDord-c3f1ded5b6c44b689150b469866de505
Source noteuspto-grants-2016_04