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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1524245Generated: October 27, 2026

Sodium Carbonate → 2-[1-Methyl-3-(trifluoromethyl)pyrazol-5-yl]-5-nitro-1,3-thiazole

https://huagongshe.com/reaction/1524245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Bromo-5-nitrothiazoleHCID 18211—
Reactant1-Methyl-3-(trifluoroMethyl)pyrazole-5-boronic acidHCID 12056713—
ReactantBrine ethyl acetateHCID 131718255—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-[1-Methyl-3-(trifluoromethyl)pyrazol-5-yl]-5-nitro-1,3-thiazoleHCID 6678015113.5%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 2-bromo-5-nitrothiazole (209 mg, 1 mmol), (1-methyl-3-(trifluoromethyl)-1H-pyrazol-5-yl)boronic acid (194 mg, 1 mmol), tetrakis(triphenylphosphine)-palladium(0) (Pd(Ph3P)4, 57 mg) and sodium carbonate (212 mg) in 3 ml DME, 0.5 ml EtOH and 0.5 ml water was heated under Ar in microwave reactor at 110° C. for 30 min. The reaction mixture was worked up with EA/brine. Org. phase was concentrated and then subjected to silica gel flash chromatography (0-30% B; A: hexane; B: 50% EA in hexane) to furnish 37.5 mg of 2-[1-methyl-3-(trifluoromethyl)pyrazol-5-yl]-5-nitro-1,3-thiazole (65) as light yellow solid (yield: 13.5%; purity>90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09079891B2
Source datasetuspto-grants-2015_07
ORD IDord-ec30b49398c340d3b52e48e0c7824a42
Source noteuspto-grants-2015_07