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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 710628Generated: November 1, 2026

1-(4-fluorophenyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-b]pyridine → HCID 86711669, compound

https://huagongshe.com/reaction/710628

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(4-fluorophenyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-b]pyridineHCID 67984610—
ReactantHCID 86711670HCID 86711670—
SolventChloroformHCID 6212—
ProductHCID 86711669HCID 86711669—

Reaction Steps

The title compound was prepared from 2-(5-methyl-3-(trifluoromethyl)-1H-1,2,4-triazol-1-yl)acetic acid and 1-(4-fluorophenyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-b]pyridine using General Method B. The product mixture was diluted with 1 mL of CHCl3 and washed with H2O. The organic layer was concentrated and the residue was purified by reverse phase HPLC (C18 column, acetonitrile-H2O with 0.1% TFA as eluent) to provide 37 mg of the title compound as a white solid. 1H NMR (400 MHz, CDCl3, mixture of rotamers) δ 8.34 (s, 0.8H), 7.59 (s, 0.2H), 7.44-7.50 (m, 2H), 7.14-7.27 (m, 2H), 5.29 (s, 0.4H), 5.18 (s, 1.6H), 3.93 (m, 0.4H), 3.86 (m, 1.6H), 2.88 (m, 2H), 2.56 (s, 2.4H), 2.55 (m, 0.6H), 2.14 (m, 1.6H), 2.06 (m, 0.4H); MS: (ES) m/z calculated for C18H17F4N6O [M+H]+ 409.1, found 409.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181241B2
Source datasetuspto-grants-2015_11
ORD IDord-19946aa9f20a49f099bf7835fc8d80f3
Source noteuspto-grants-2015_11