HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887613Generated: October 30, 2026
4-Tert-Butylaniline → N-(4-(Tert-butyl)phenyl)-5-chloro-1-methyl-1H-pyrazole-4-carboxamide
https://huagongshe.com/reaction/887613
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Tert-Butylaniline | HCID 69861 | — |
| Reactant | 5-Chloro-1-methyl-1H-pyrazole-4-carbonyl chloride | HCID 2735773 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(4-(Tert-butyl)phenyl)-5-chloro-1-methyl-1H-pyrazole-4-carboxamide | HCID 86588705 | — |
Reaction Steps
5-Chloro-1-methyl-1H-pyrazole-4-carbonyl chloride (1.0 g, 5.6 mmol) was dissolved in CH2Cl2 (100 mL) under N2 and cooled to 0° C. 4-t-Butylaniline was added and the reaction was stirred with gradual warming to RT overnight. The reaction was quenched with saturated NaHCO3(aq) and extracted 3× with fresh CH2Cl2. The CH2Cl2 extracts were washed with brine, combined, dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure giving 5-chloro-1-methyl-1H-pyrazole-4-carboxylic acid (4-tert-butyl-phenyl)-amide as a foamy pink solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08247430B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-51a129c9e3f24786a30dcc5648849b96 |
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| Source note | uspto-grants-2012_08 |
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