HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520282Generated: November 4, 2026
Hydrochloric Acid → 4-((4,4,4-trifluoro-1-(2-methyl-4-(4,5,6,7-tetrahydro-2H-indazol-2-yl)phenyl)butyl)amino)benzoic acid
https://huagongshe.com/reaction/1520282
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | methyl 4-((4,4,4-trifluoro-1-(2-methyl-4-(4,5,6,7-tetrahydro-2H-indazol-2-yl)phenyl)butyl)amino)benzoate | HCID 117840555 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-((4,4,4-trifluoro-1-(2-methyl-4-(4,5,6,7-tetrahydro-2H-indazol-2-yl)phenyl)butyl)amino)benzoic acid | HCID 117840354 | — |
Reaction Steps
To a mixture of methyl 4-((4,4,4-trifluoro-1-(2-methyl-4-(4,5,6,7-tetrahydro-2H-indazol-2-yl)phenyl)butyl)amino)benzoate (8.01 g), THF (34 mL) and methanol (34 mL) was added 1M aqueous sodium hydroxide solution (68 mL), and the mixture was stirred at 50° C. overnight. To the reaction mixture was added THF (34 ml), and the mixture was stirred at 60° C. for 7 hr. The reaction mixture was neutralized with 1M hydrochloric acid (68 mL), and extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give the title compound as a crudely purified product. This compound was used in step C without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09073864B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-fccd6414797a46508bf7c7234917914d |
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| Source note | uspto-grants-2015_07 |
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