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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2267964Generated: October 30, 2026

Pyridine → HCID 18348179, compound

https://huagongshe.com/reaction/2267964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant1-(Bis(4-fluorophenyl)methyl)piperazineHCID 152932—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 18348175HCID 18348175—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 18348179HCID 1834817953.6%

Reaction Steps

Under a nitrogen atmosphere a 15 mL solution of 2-methylindol-3-ylacetyl chloride (0.013 mole) in tetrahydrofuran was added to a stirred solution of 3.9 grams (0.014 mole) of N-[bis(4-fluorophenyl)methyl]piperazine and 1.1 mL (0.013 mole) of pyridine in 50 mL of dried tetrahydrofuran. Upon completion of the addition the reaction mixture was stirred at ambient temperature for about 18 hours, after which the reaction mixture was poured into a mixture of 200 mL of ethyl acetate and 100 mL of aqueous saturated sodium bicarbonate solution. The organic layer was separated and washed with one portion of a saturated sodium chloride solution, dried with sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure to a solid, which was taken up in hexane. This solution was concentrated under reduced pressure, yielding 3.2 grams of N-(2-methylindol-3-ylacetyl)-N′-[bis(4-fluorophenyl)methyl]piperazine, mp 93-103° C. The NMR spectrum was consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSH0002007H1
Source datasetuspto-grants-2001_12
ORD IDord-46f8eed382604ce0ac04a0da02c41454
Source noteuspto-grants-2001_12