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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108100Generated: November 1, 2026

Hydrochloric Acid → HCID 23045035, compound

https://huagongshe.com/reaction/2108100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantQuinaldic AcidHCID 7124—
ReactantDiethyl cyanophosphonateHCID 76257—
Reactant1-[(3,4,5-Trimethoxyphenyl)methyl]piperazine;dihydrochlorideHCID 12828501—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
ProductHCID 23045035HCID 2304503549.9%

Reaction Steps

To a mixture of 2-quinolinecarboxylic acid (0.55 g), 1-(3,4,5-trimethoxybenzyl)piperazine dihydrochloride (1.1 g), triethylamine (1.2 g) and N,N-dimethylformamide (20 ml) is added dropwise at room temperature diethyl cyanophosphonate (1.2 ml), followed by stirring for one hour. After addition of water (100 ml) and ethyl acetate (100 ml), the reaction mixture is extracted with ethyl acetate. The extract is washed with water, dried, and concentrated under reduced pressure. The residue is purified by means of a silica gel column chromatography (hexane:acetone=2:1-1:1) to give an oily product, which is led to its hydrochloride, followed by crystallizing from a mixture of methanol, ethyl acetate and ethyl ether to give 1-(2-quinolylcarbonyl)-4-(3,4,5-trimethoxybenzyl)piperazine dihydrochloride (0.4 g) as colorless crystals, m.p. 151°-155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04937246
Source datasetuspto-grants-1990_06
ORD IDord-e29667f649a34a87ae0ab5dc1d741b1a
Source noteuspto-grants-1990_06