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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301374Generated: October 31, 2026

O-Methylhydroxylamine hydrochloride → HCID 178502870, compound

https://huagongshe.com/reaction/2301374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
ReactantHCID 54383158HCID 54383158—
SolventMethanolHCID 887—
ProductHCID 178502870HCID 17850287027.2%

Reaction Steps

To a stirred solution of 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-methylsulfinyl-1H-pyrazole-3-carboximidic acid methyl ester (1.0 g) in anhydrous methanol was added anhydrous methoxylamine hydrochloride (0.2 g). After 4 hours at 20° C., the mixture was evaporated and dichloromethane and water added. The organic layer was dried (MgSO4), evaporated and chromatographed on a florisil column, eluting with 3:1 dichloromethane/ethyl acetate to give 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-N-methoxy-4-methylsulfinyl-1H-pyrazole-3-carboximidamide(0.28 g),m.p. 140-145° C.Compound 49. By proceeding in a similar manner the following compounds were prepared:5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-N-methoxy-4-trifluoromethylsulfinyl-1H-pyrazole-3-carboximidamide, m.p.169-170° C. Compound 41.; and 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-N-hydroxy4-trifluoromethylsulfinyl-1H-pyrazole-3-carboximidamide, m.p.222-224° C. Compound 40.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500850B2
Source datasetuspto-grants-2002_12
ORD IDord-dad6d7c051284a62bfb82c5c6a2dcbd3
Source noteuspto-grants-2002_12