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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802777Generated: November 2, 2026

Sodium triacetoxyborohydride → 3-{2-[2-(4-Bromo-phenyl)-4-methyl-piperazin-1-yl]-ethyl}-pyrazolo[1,5-a]pyridine

https://huagongshe.com/reaction/1802777

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant3-(4-Bromo-phenyl)-1-methyl-piperazineHCID 57899227—
Reactant2-{Pyrazolo[1,5-a]pyridin-3-yl}acetaldehydeHCID 57899252—
CatalystAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product3-{2-[2-(4-Bromo-phenyl)-4-methyl-piperazin-1-yl]-ethyl}-pyrazolo[1,5-a]pyridineHCID 5789924750.2%

Reaction Steps

To a solution of 3-(4-bromo-phenyl)-1-methyl-piperazine (1.0 g, 3.92 mmol), pyrazolo[1,5-a]pyridin-3-yl-acetaldehyde (753 mg, 4.70 mmol) and acetic acid (1.2 mg) in tetrahydrofuran (15 mL) was added sodium triacetoxyborohydride (1.92 g, 8.62 mmol) and the resulting mixture was stirred at room temperature for 4 h. The reaction mixture was diluted with ethyl acetate, washed with a saturated aqueous sodium bicarbonate solution, a saturated aqueous solution of sodium chloride, dried over magnesium sulfate, filtered and concentrated in vacuo. Purification via flash silica gel column chromatography (heptane/ethyl acetate) gave 3-{2-[2-(4-bromo-phenyl)-4-methyl-piperazin-1-yl]-ethyl}-pyrazolo[1,5-a]pyridine (786 mg, 50% yield). LCMS (m/z): 401.00 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349883B2
Source datasetuspto-grants-2013_01
ORD IDord-fc6399ecd6c049c9baadc29b2950b90b
Source noteuspto-grants-2013_01