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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445540Generated: October 31, 2026

Methylamine → 1-(3-Chloro-2-pyridinyl)-N-[2,4-dichloro-6-[(methylamino)carbonyl]phenyl]-3-[(methylsulfonyl)oxy]-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/1445540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylamineHCID 6329—
Reactant6,8-dichloro-2-[1-(3-chloro-2-pyridinyl)-3-[(methylsulfonyl)oxy]-1H-pyrazol-5-yl]-4H-3,1-benzoxazin-4-oneHCID 86602663—
SolventAcetonitrileHCID 6342—
Product1-(3-Chloro-2-pyridinyl)-N-[2,4-dichloro-6-[(methylamino)carbonyl]phenyl]-3-[(methylsulfonyl)oxy]-1H-pyrazole-5-carboxamideHCID 86602662—

Reaction Steps

To a solution of 6,8-dichloro-2-[1-(3-chloro-2-pyridinyl)-3-[(methylsulfonyl)oxy]-1H-pyrazol-5-yl]-4H-3,1-benzoxazin-4-one (i.e. the product of step D) (0.05 g, 0.10 mmol) in acetonitrile (3 mL) was added methylamine (2.0 M solution in THF, 0.5 mL, 1 mmol). The resulting solution was stirred at room temperature overnight. Thin layer chromatography showed the reaction to be incomplete. Methylamine (2.0 M solution in THF, 0.5 mL, 1 mmol) was added dropwise and the reaction stirred 1 hour at room temperature. Thin layer chromatography showed the reaction was complete. The reaction mixture was concentrated to dryness to yield 0.057 g of the title compound, a compound of present invention, as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666882B2
Source datasetuspto-grants-2010_02
ORD IDord-0bad6fd453fd49bdb9f0c3d426978113
Source noteuspto-grants-2010_02