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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1269756Generated: November 1, 2026

Trifluoroacetic acid → HCID 22933906, compound

https://huagongshe.com/reaction/1269756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 178454038HCID 178454038—
ProductHCID 22933906HCID 2293390683%

Reaction Steps

Trifluoroacetic acid (6.0 ml) was added to the trans-tert-butyl-4-[(1H-indazol-5-ylcarbonyl)amino]cyclo-hexylcarbamate (420 mg, 1.17 mmol) obtained in Example 158, and the resulting mixture was stirred at room temperature for 1 hour. After the reaction solution was concentrated under reduced pressure, ethanol (10 ml) was added to the concentration residue, followed by washing by repulping. The residue washed was filtered and then dried under reduced pressure to obtain N-(4-aminocyclohexyl)-1H-indazole-5-carboxamide trifluoroacetate (363 mg, 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07199147B2
Source datasetuspto-grants-2007_04
ORD IDord-acd119c442bd4c87b7cef16235d5e5a7
Source noteuspto-grants-2007_04