Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478082Generated: October 30, 2026

Trifluoroacetic acid → HCID 118390074, compound

https://huagongshe.com/reaction/1478082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium CarbonateHCID 10340—
Reactant1,5-Dimethyl-1H-pyrazol-4-amine--hydrogen chloride (1/1)HCID 46737045—
Reactanttert-butyl 5-((2,5-dichloropyrimidin-4-yl)amino)hexahydrocyclopenta[c]pyrrole-2(1H)-carboxylateHCID 118389983—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 118390074HCID 11839007419.6%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a suspension of tert-butyl 5-((2,5-dichloropyrimidin-4-yl)amino)hexahydrocyclopenta[c]pyrrole-2(1H)-carboxylate (579.1 mg, 1.55 mmol) and 1,5-dimethylpyrazol-4-amine hydrochloride (446.8 mg, 3.03 mmol) in dioxane (10 mL) was added trifluoroacetic acid (862.8 mg, 7.57 mmol). The reaction mixture was stirred at 100° C. overnight and adjusted to pH=10 with a saturated Na2CO3 solution, then extracted with DCM (100 mL×3). The combined organic phases were washed with brine (100 mL), dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The residue was purified by silica gel column chromatography (MeOH/DCM=1/10) to give the title compound as a beige solid (105.6 mg, 19.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403801B2
Source datasetuspto-grants-2016_08
ORD IDord-767b7654f6524f418ade583e8ff9ae35
Source noteuspto-grants-2016_08