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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2427016Generated: November 1, 2026

Acetonitrile → 6-chloro-2-[1-(2-chlorophenyl)-3-trifluoromethyl-1H-pyrazol-5-yl]-8-methyl-4H-3,1-benzoxazine-4-one

https://huagongshe.com/reaction/2427016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-Amino-5-chloro-3-methylbenzoic acidHCID 11644044—
Reactant2-(2-Chloro-phenyl)-5-trifluoromethyl-2H-pyrazole-3-carbonyl chlorideHCID 57458238—
SolventTriethylamineHCID 8471—
Product6-chloro-2-[1-(2-chlorophenyl)-3-trifluoromethyl-1H-pyrazol-5-yl]-8-methyl-4H-3,1-benzoxazine-4-oneHCID 6685456868.9%

Reaction Steps

To a mixture of 1.0 g of 1-(2-chlorophenyl)-3-trifluoromethyl-1H-pyrazole-5-carbonyl chloride and 10 ml of acetonitrile was added 0.60 g of 2-amino-5-chloro-3-methylbenzoic acid, and the resulting mixture was stirred at room temperature for 10 minutes. To the mixture, 0.46 ml of triethylamine was added. After the mixture was stirred at room temperature for 20 minutes, 0.92 ml of triethylamine was further added thereto. After the mixture was stirred at room temperature for 20 minutes, 0.28 ml of methanesulfonyl chloride was added thereto and the mixture was stirred at room temperature for 3 hours. The reaction mixture was filtered, and the resulting filtrate was concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography to obtain 0.98 g of 6-chloro-2-[1-(2-chlorophenyl)-3-trifluoromethyl-1H-pyrazol-5-yl]-8-methyl-4H-3,1-benzoxazine-4-one of the formula:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968573B2
Source datasetuspto-grants-2011_06
ORD IDord-dca1628bfaff4eff901ad52175a991b7
Source noteuspto-grants-2011_06