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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480395Generated: November 3, 2026

Diisopropylethylamine → Heteroaromatic ring derivative 2

https://huagongshe.com/reaction/1480395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPropylphosphonic anhydrideHCID 111923—
Reactant3,5-Dichlorobenzyl 4-aminopiperidine-1-carboxylate hydrochlorideHCID 86722638—
ReactantHCID 178525383HCID 178525383—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHeteroaromatic ring derivative 2HCID 178520559—

Reaction Steps

4-(1H-1,2,3-Triazol-4-yl)butanoic acid (step 4) (882 mg, 4.95 mmol) and 3,5-dichlorobenzyl 4-aminopiperidine-1-carboxylate hydrochloride (step 2) (1.5 g, 4.95 mmol) were suspended in DMF (20 ml). DIPEA (4.32 ml, 24.74 mmol) was added and the reaction mixture stirred until all components were in solution. 50% T3P® solution in DMF (5.78 ml, 9.89 mmol) was added and the reaction mixture was stirred at RT for 48 hrs. The reaction mixture was diluted with EtOAc and washed twice with 10% citric acid. The aqueous citric acid wash was extracted with DCM (3×) and the combined extracted were dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography, using a gradient solvent system of 0-10% MeOH in EtOAc. The resulting product was further purified by stirring in diethyl ether over 72 hours. The mixture was filtered and the solid was dried in a vacuum oven to afford the title compound;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409895B2
Source datasetuspto-grants-2016_08
ORD IDord-53109008fa7b445199e3f67000964bbd
Source noteuspto-grants-2016_08