HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245657Generated: October 29, 2026
Triethylamine → N-((3-chloropyrazin-2-yl)methyl)-4-oxocyclohexanecarboxamide
https://huagongshe.com/reaction/245657
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Oxocyclohexanecarboxylate | HCID 5460131 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | (3-Chloropyrazin-2-yl)methanamine hydrochloride | HCID 42614233 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-((3-chloropyrazin-2-yl)methyl)-4-oxocyclohexanecarboxamide | HCID 86674630 | 104.7% |
Reaction Steps
To a stirred suspension of 2-aminomethyl-3-chloropyrazine hydrochloride (3.89 mmol, 0.70 g) in dichloromethane (25 mL) at room temperature was subsequently added triethylamine (7.78 mmol, 1.08 mL), O-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluroniumhexafluorophosphate (4.67 mmol, 1.77 g) and finally 4-oxocyclohexanecarboxylate (3.89 mmol, 553 mg). After stirring for 16 hours, the suspension filtered over decalite. The decalite was washed with dichloromethane. The filtrate was washed with water, dried (sodium sulfate) and concentrated in vacuo. The resulting crude product was purified by column chromatography on silica gel (ethyl acetate). The product was dissolved in dichloromethane, washed with water and concentrated in vacuo to afford 1.09 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658794B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-aa3acf190c714b1faa396a1e1c0a9852 |
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| Source note | uspto-grants-2014_02 |
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