HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706685Generated: October 29, 2026
Sulfuric Acid → 5-chloro-1-(3-(trifluoromethyl)benzyl)-1H-indazol-4-amine
https://huagongshe.com/reaction/706685
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 1-(3-(trifluoromethyl)benzyl)-1H-indazol-4-amine | HCID 67976355 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-chloro-1-(3-(trifluoromethyl)benzyl)-1H-indazol-4-amine | HCID 67976421 | — |
Reaction Steps
A solution of 1-(3-(trifluoromethyl)benzyl)-1H-indazol-4-amine (0.056 g, 0.192 mmol) in THF (1.0 mL) was cooled to −78° C. under N2. H2SO4 (0.00512 mL, 0.0961 mmol) was added and the mixture was stirred for 5 minutes. N-chlorosuccinimide (0.0257 g, 0.192 mmol) was added in one portion and the reaction was stirred at −78° C. for 1 hour. Sodium carbonate (0.0204 g, 0.192 mmol) was added and the mixture was warmed to ambient temperature. The mixture was diluted with water (5 mL) and extracted with EtOAc (3×10 mL). The combined organic layers were then washed with brine and dried over Na2SO4, filtered and concentrated. The crude product was purified by preparative TLC (40% EtOAc/hexane) in which two major bands were observed. The higher band was determined to be the title compound (0.028 g, 44%) and was isolated as a dark yellow/green solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09174981B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-3afc3dbc1e994d3ab9c7ceda564b9249 |
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| Source note | uspto-grants-2015_11 |
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