HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570998Generated: October 26, 2026
Pyrazole → N,N-dimethyl-1H-pyrazole-1-sulfonamide
https://huagongshe.com/reaction/570998
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyrazole | HCID 1048 | — |
| Reactant | 3-Bromopyridine | HCID 12286 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Dimethylsulphamoyl chloride | HCID 83372 | — |
| Reactant | 3-(3-chloro-1H-pyrazol-1-yl)pyridine | HCID 67499540 | — |
| Reactant | HCID 178478253 | HCID 178478253 | — |
| Product | N,N-dimethyl-1H-pyrazole-1-sulfonamide | HCID 10954038 | — |
| Product | HCID 178478253 | HCID 178478253 | — |
Reaction Steps
US 20130288893(A1) describes, inter alia, certain (3-halo-1-(pyridin-3-yl)-1H-pyrazol-4-yl)amides and carbamates and their use as pesticides. The route to prepare such compounds involved the preparation of 3-(3-chloro-1H-pyrazol-1-yl)pyridine by the direct coupling of 3-bromopyridine with 3-chloropyrazole. The 3-chloropyrazole was prepared by a) treating 1H-pyrazole with 2 dimethylsulfamoyl chloride and sodium hydride to provide N,N-dimethyl-1H-pyrazole-1-sulfonamide, b) treating the N,N-dimethyl-1H-pyrazole-1-sulfonamide with perchloroethane and n-butyl lithium to provide 3-chloro-N,N-dimethyl-1H-pyrazole-1-sulfonamide, and c) removing the N,N-dimethylsulfonamide from 3-chloro-N,N-dimethyl-1H-pyrazole-1-sulfonamide with trifluoroacetic acid to give the 3-chloropyrazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09024031B1 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-2a03cfb05023492ca6503b714575bfc6 |
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| Source note | uspto-grants-2015_05 |
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