HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852794Generated: October 26, 2026
N-Methylethylamine → HCID 178464470, compound
https://huagongshe.com/reaction/1852794
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylethylamine | HCID 12219 | — |
| Reactant | Propylphosphoric anhydride | HCID 16167369 | — |
| Reactant | HCID 178461212 | HCID 178461212 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178464470 | HCID 178464470 | — |
Reaction Steps
To a reaction vessel was added the crude residue of (S)-1-(4-(5-chloropyridin-3-yl)-6-cyano-3-((trans-4-methylcyclohexyl)methyl)-3H-imidazo[4,5-c]pyridin-2-yl)pyrrolidine-2-carboxylic acid (0.030 g, 0.063 mmol), propylphosphonic anhydride (0.10 mL, 50% w/w in DMF), and N-methylethanamine (0.0037 g, 0.063 mmol) suspended in DMF (0.5 mL). The reaction was stirred at ambient temperature for 6 hours. The reaction was diluted with H2O (2.0 mL) and was extracted with EtOAc (2×5 mL). The combined organics were concentrated in vacuo to afford (S)-1-(4-(5-chloropyridin-3-yl)-6-cyano-3-((trans-4-methylcyclohexyl)methyl)-3H-imidazo[4,5-c]pyridin-2-yl)-N-ethyl-N-methylpyrrolidine-2-carboxamide as a crude residue. MS ESI calc'd. for C28H34ClN7O [M+H]+ 520. found 520.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962611B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-e5ea22cb756246229eb4f0dbe442994e |
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| Source note | uspto-grants-2015_02 |
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