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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502998Generated: November 3, 2026

Amantadine → HCID 68469414, compound

https://huagongshe.com/reaction/502998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmantadineHCID 2130—
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBroPHCID 2733179—
ReactantHCID 68466046HCID 68466046—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductHCID 68469414HCID 6846941472.8%

Reaction Steps

1-[5-(2-Chlorophenyl)-4-methyl-1,2,4-triazol-3-yl]cyclobutanecarboxylic acid (200 mg) was suspended in methylene chloride (7 ml) and then diisopropylethylamine (0.72 ml) and bromotris(pyrrolidino)phosphonium hexafluorophosphate salt (416 mg) were added thereto, followed by stirring at room temperature for 30 minutes. Then, 1-adamantanamine (104 mg) was added to the reaction solution and the whole was stirred at room temperature for 15 hours. The reaction solution was diluted with a saturated aqueous sodium bicarbonate solution (30 ml), followed by extraction with chloroform (20 ml×2). The organic layer was dried over anhydrous sodium sulfate and filtrated and then the solvent was removed by evaporation under reduced pressure. The resulting residue was purified by column chromatography (methanol:chloroform=2:98) and the resulting solid washed with hexane and diethyl ether to obtain 212 mg of N-1-adamantyl-1-[5-(2-chlorophenyl)-4-methyl-1,2,4-triazol-3-yl]cyclobutanecarboxamide (white solid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776897B2
Source datasetuspto-grants-2010_08
ORD IDord-2e80c2d0aca6479f9b32938c98f950b8
Source noteuspto-grants-2010_08