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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 660124Generated: November 1, 2026

Water → 2-(3-Chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazole-3-carboxylic acid [4-chloro-2-methyl-6-(3-methyl-thietan-3-ylcarbamoyl)-phenyl]-amide

https://huagongshe.com/reaction/660124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant6-chloro-2-[2-(3-chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazol-3-yl]-8-methylbenzo[d][1,3]oxazin-4-oneHCID 23150351—
Reactant3-Methylthietan-3-amineHCID 55281677—
SolventTetrahydrofuranHCID 8028—
Product2-(3-Chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazole-3-carboxylic acid [4-chloro-2-methyl-6-(3-methyl-thietan-3-ylcarbamoyl)-phenyl]-amideHCID 5939358540%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 6-chloro-2-[1-(3-chloro-2-pyridinyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl]-8-methyl-4H-3,1-benzoxazin-4-one (1.13 g, 2.56 mmol) (prepared according to WO 02/48115, example 2D) in tetrahydrofuran (15 ml) is added 3-amino-3-methyl-thietane (the product of step 3) (0.66 g, 6.40 mmol), and the mixture is heated for 48 hours at 50° C., then to reflux for 12 hours. The cooled reaction mixture is poured into water, extracted with ethyl acetate, the combined organic layers washed with water and brine, dried (Na2SO4), filtered, and concentrated. The crude product is purified by flash chromatography (ethyl acetate/hexane 1:2) to afford 560 mg (40%) of the title compound as a white solid, m.p. 238-241° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084474B2
Source datasetuspto-grants-2011_12
ORD IDord-8c1ca71d6ef74173a4af3f5c8b120ab3
Source noteuspto-grants-2011_12