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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868473Generated: November 2, 2026

Potassium Carbonate → Tert-butyl 5-(2,4-dichlorophenyl)-7-methyl-2-(oxazol-5-yl)imidazo[1,2-a]pyrimidine-6-carboxylate

https://huagongshe.com/reaction/1868473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTosylmethyl isocyanideHCID 161915—
ReactantTert-butyl 5-(2,4-dichlorophenyl)-2-formyl-7-methylimidazo[1,2-a]pyrimidine-6-carboxylateHCID 57982513—
SolventMethanolHCID 887—
ProductTert-butyl 5-(2,4-dichlorophenyl)-7-methyl-2-(oxazol-5-yl)imidazo[1,2-a]pyrimidine-6-carboxylateHCID 5798254366.3%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of tert-butyl 5-(2,4-dichlorophenyl)-2-formyl-7-methylimidazo[1,2-a]pyrimidine-6-carboxylate (90 mg, 0.22 mmol) in MeOH (4 mL) was added tosyl methyl isocyanide (52 mg, 0.27 mmol) and K2CO3 (61 mg, 0.44 mmol). After heating to 60° C. for 30 min, the reaction was concentrated under reduced pressure and purified by silica gel chromatography to provide tert-butyl 5-(2,4-dichlorophenyl)-7-methyl-2-(oxazol-5-yl)imidazo[1,2-a]pyrimidine-6-carboxylate (65 mg, 66%) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635699B2
Source datasetuspto-grants-2009_12
ORD IDord-8b1d3b35899742a999db2e423e3e861d
Source noteuspto-grants-2009_12