HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192806Generated: October 30, 2026
1,2-Dichloroethane → HCID 59625331, compound
https://huagongshe.com/reaction/2192806
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Chloro-N,N,N',N'-tetramethylformamidinium Hexafluorophosphate | HCID 10989639 | — |
| Reactant | HCID 59625412 | HCID 59625412 | — |
| Reactant | HCID 59625616 | HCID 59625616 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 59625331 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329691B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-7900202318e4429485bd03378be85890 |
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| Source note | uspto-grants-2012_12 |
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