HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425480Generated: October 28, 2026
Dimethylamine → 5-chloro-N,N-dimethylpyrazine-2-carboxamide
https://huagongshe.com/reaction/2425480
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 5-Chloropyrazinoic acid | HCID 465472 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-chloro-N,N-dimethylpyrazine-2-carboxamide | HCID 59000470 | — |
Reaction Steps
Oxalyl chloride (1.7 mL, 19 mmol) was added to a suspension of 5-chloropyrazine-2-carboxylic acid (CAS no. 36070-80-1) (2.53 g, 16.0 mmol) in dichloromethane (25 mL) and DMF (4 drops) at RT and under argon. The mixture was allowed to stir for 1.5 h, concentrated in vacuo to and the residue was re-dissolved in dichloromethane (25 mL). Dimethylamine (2M in THF, 8.77 mL, 17.6 mmol) was then added dropwise followed by triethylamine (4.9 mL, 35 mmol) and allowed to stir for a further 5.5 hours. The reaction mixture was concentrated in vacuo and the residue was re-dissolved in dichloromethane and filtered. The filtrate was chromatographed on silica, eluting with a gradient of 50-100% ethyl acetate in isohexanes to give the desired compound (1.88 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07964725B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-01594a91a17c4a54bf777a9abf925e2b |
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| Source note | uspto-grants-2011_06 |
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