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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200945Generated: October 26, 2026

Pyridine → HCID 66627850, compound

https://huagongshe.com/reaction/2200945

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant1-Fluorocyclopropanecarbonyl chlorideHCID 54101822—
Reactant(7R)-2-amino-7-(4-cyanophenyl)-5-methyl-4-[3-(trifluoromethyl)phenyl]-4,7-dihydro[1,2,4]triazolo[1,5-a]pyrimidine-6-carbonitrile hydrochlorideHCID 66627899—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66627850HCID 66627850—

Reaction Steps

Under an atmosphere of argon protective gas, (7R)-2-amino-7-(4-cyanophenyl)-5-methyl-4-[3-(trifluoromethyl)phenyl]-4,7-dihydro[1,2,4]triazolo[1,5-a]pyrimidine-6-carbonitrile hydrochloride (30 mg, 66 μmol) was dissolved in abs. pyridine (1.5 ml). At room temperature, 1-fluorocyclopropanecarbonyl chloride (20 mg, 165 μmol, 2.5 eq.) in abs. THF (1 ml) was added in two portions, and the mixture was stirred for 12 h. The reaction mixture was then concentrated under reduced pressure and directly purified by preparative HPLC (Kromasil C18 column, 5 μm, 50×20 mm; mobile phase: acetonitrile-water-0.1% TFA). After lyophilization, the product was obtained as a solid (29.5 mg, 89% of theory).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359362B2
Source datasetuspto-grants-2016_06
ORD IDord-83226b0128524fcfa0b941b196a5e0ca
Source noteuspto-grants-2016_06