HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989233Generated: November 1, 2026
O-Methylhydroxylamine hydrochloride → HCID 178502870, compound
https://huagongshe.com/reaction/989233
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | HCID 54383158 | HCID 54383158 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178502870 | HCID 178502870 | 27.2% |
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-hydroxy-4-trifluoromethylsulfinyl-1H-pyrazole-3-carboximidamide, m.p.222-224° C. Compound 40.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06638956B2 |
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| Source dataset | uspto-grants-2003_10 |
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| ORD ID | ord-86b38d6586694c6b9cb59d1f3108e41b |
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| Source note | uspto-grants-2003_10 |
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