HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2233918Generated: October 30, 2026
1,2-Dichloroethane → 2-Chloro-6-(4-{[(4-cyano-5-methyl-1H-pyrrol-2-yl)carbonyl]amino}piperidin-1-yl)isonicotinamide
https://huagongshe.com/reaction/2233918
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | 4-Cyano-5-methyl-1H-pyrrole-2-carboxylic acid | HCID 59864736 | — |
| Reactant | 2-(4-Aminopiperidin-1-yl)-6-chloroisonicotinamide hydrochloride | HCID 86608255 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Chloro-6-(4-{[(4-cyano-5-methyl-1H-pyrrol-2-yl)carbonyl]amino}piperidin-1-yl)isonicotinamide | HCID 57396007 | 7.2% |
Reaction Steps
Diisopropylethylamine (0.1 ml, 0.56 mmol), EDC (0.09 g, 0.46 mmol) and HOAT (0.064 g, 0.46 mmol) were added to a stirred solution of 4-cyano-5-methyl-1H-pyrrole-2-carboxylic acid (Intermediate 13, 0.07 g, 0.47 mmol) in DMF (1.5 ml) at room temperature. The resultant solution was stirred for 30 mins and a solution of 2-(4-aminopiperidin-1-yl)-6-chloroisonicotinamide hydrochloride (Intermediate 70, 0.16 g, 0.56 mmol) in 1 ml of DMF was added. The reaction was stirred overnight, then concentrated under vacuum and the residue was partitioned between water and EtOAc. The aqueous layer was extracted with EtOAc (×2) and the combined organic extracts were washed with 1 N HCl, water and brine, dried over MgSO4 and concentrated under vacuum. The residue was purified by reverse phase chromatography to give the desired product as a white solid (13 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07709503B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-f75de6db6527438f9832fa3ac09081ec |
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| Source note | uspto-grants-2010_05 |
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