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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192806Generated: October 30, 2026

1,2-Dichloroethane → HCID 59625331, compound

https://huagongshe.com/reaction/2192806

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantDiisopropylethylamineHCID 81531—
ReactantChloro-N,N,N',N'-tetramethylformamidinium HexafluorophosphateHCID 10989639—
ReactantHCID 59625412HCID 59625412—
ReactantHCID 59625616HCID 59625616—
SolventSodium BicarbonateHCID 516892—
ProductHCID 59625331HCID 59625331—

Reaction Steps

2-[(Furan-2-ylmethyl)amino]-7,7-dimethyl-6,7-dihydro-5H-cyclopenta[b]pyridine-3-carboxylic acid (390 mg), tert-butyl 3-[(2-methylpropyl)amino]piperidine-1-carboxylate (350 mg) and N,N-diisopropylethylamine (1.2 ml) were dissolved in 1,2-dichloroethane (10 ml), chloro-N,N,N′,N′-tetramethylformamidinium hexafluorophosphate (540 mg) was added and the mixture was stirred at room temperature for 18 hr. The reaction mixture was diluted with saturated aqueous sodium hydrogen carbonate solution and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography, and the fraction eluted with ethyl acetate-hexane (5:95-100:10) was concentrated under reduced pressure to give the object compound (123 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329691B2
Source datasetuspto-grants-2012_12
ORD IDord-7900202318e4429485bd03378be85890
Source noteuspto-grants-2012_12