HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099037Generated: November 3, 2026
Ammonia → 5-Amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-4-((trifluoromethyl)thio)-1H-pyrazole-3-carboxamide
https://huagongshe.com/reaction/2099037
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonia | HCID 222 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 5-Amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-(trifluoromethylsulfanyl)pyrazole-3-carboxylic acid | HCID 22618497 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Amino-1-(2,6-dichloro-4-(trifluoromethyl)phenyl)-4-((trifluoromethyl)thio)-1H-pyrazole-3-carboxamide | HCID 86613234 | 98% |
Reaction Steps
A mixture of 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-trifluoromethylthio-1H-pyrazole-3-carboxylic acid (1.00 g, 2.27 mmol) and 1,1-dicarbonylimidazole (0.45 g, 2.72 mmol) in dioxane was heated to 50° C. for 2 hours. An aqueous solution of ammonia (33%, 80 ml) was then added and stirring continued at 50° C. for 4 hours. The cooled mixture was diluted with water and extracted with ethyl acetate/heptane (1:1). The combined organic phase was washed with aqueous potassium hydrogensulfate (5%), dried over magnesium sulfate and evaporated to give the title compound (0.980 g, yield 98%) as a white foam, 1H NMR (CDCl3): 4.36 (bs, 2H, NH2), 5.60 and 6.69 (bs, 2H, C(O)NH2), and 7.82 (s, 2H, Ar—H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07569516B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-0a05a9f7d6bb4a008ed49a3fc590fad7 |
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| Source note | uspto-grants-2009_08 |
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