HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25241Generated: October 26, 2026
Diisopropylethylamine → HCID 178473534, compound
https://huagongshe.com/reaction/25241
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Chloro-1-methylpyridinium iodide | HCID 167069 | — |
| Reactant | Ethyl (morpholin-4-ylcarbonothioyl)carbamate | HCID 2824559 | — |
| Reactant | 2-amino-N-(-4-cyano-1-methyl-piperidin-4-yl)-3-cyclohexylpropionamide bis hydrochloride salt | HCID 22566339 | — |
| Solvent | Citric Acid | HCID 311 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178473534 | HCID 178473534 | 26% |
Reaction Steps
2-Chloro-N-methylpyridinium iodide (680 mg, 2.66 mmol), was added to a solution of (morpholine-4-carbothioyl)-carbamic acid ethyl ester (450 mg, 2.06 mmol), 2-amino-N-(4-cyano-1-methyl-piperidin-4-yl)-3-cyclohexyl-propionamide bis hydrochloride salt (745 mg, 2.04 mmol), and N,N-diisopropylethylamine (1.10 mL, 6.3 mmol) in dichloromethane (8.0 mL). The reaction was stirred at room temperature for 2.5 h then taken up in 10% citric acid solution and washed with EtOAc. The aqueous phase was then basified with saturated sodium carbonate and extracted with EtOAc. The organic extract was dried (MgSO4) and concentrated to provide the desired product as a white solid (250 mg, 26%). This material was further purified by HPLC using a 20×250 mm C18 reverse phase column with the method being 20% acetonitrile in water to 90% acetonitrile in water. MS, m/z 477=M+1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06858623B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-9b2ff7f0a0c44c8fbe2f7f2192754cef |
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| Source note | uspto-grants-2005_02 |
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