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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264347Generated: October 30, 2026

Sodium Chloride → HCID 23112209, compound

https://huagongshe.com/reaction/2264347

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
Reactant4-MethylmorpholineHCID 7972—
Reactant3-MethoxyanilineHCID 10824—
ReactantMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
ReactantHCID 23112265HCID 23112265—
Solvent1,2-DichloroethaneHCID 11—
SolventWaterHCID 962—
ProductHCID 23112209HCID 23112209—

Reaction Steps

Into 20 ml of 1,2-dichloroethane were suspended 500 mg of a mixture of 2-(piperidin-1-ylmethyl)biphenyl-4-carboxylic acid and 1.5 equivalents of sodium chloride, and then 174 mg of 3-methoxyaniline dissolved in 2 ml of 1,2-dichloroethane was added thereto. Under ice cooling, 694 mg of O-benzotriazol-1-yl-N,N,N′,N′-tetramethyluronium hexafluorophosphate and 211 μl of N-methylmorpholine were added thereto, followed by 30 hours of stirring at room temperature. Water was added to the reaction solution and the organic layer was extracted with chloroform. The organic layer was dried over anhydrous magnesium sulfate, followed by removal of the solvent by evaporation. The obtained residue was purified by silica gel column chromatography (chloroform:methanol:aqueous ammonia) to obtain N-(3-methoxyphenyl)-2-(piperidin-1-ylmethyl)biphenyl-4-carboxamide. The compound was dissolved in 3 ml of ethyl acetate and then 1 ml of a 4M ethyl acetate solution of hydrochloric acid was added thereto. The solvent was removed by evaporation and crystallization was effected from ethanol to obtain 103 mg of N-(3-methoxyphenyl)-2-(piperidin-1-ylmethyl)biphenyl-4-carboxamide hydrochloride as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855198B2
Source datasetuspto-grants-2010_12
ORD IDord-59cde8c6658c49b1808bbe2afbaf8d58
Source noteuspto-grants-2010_12