HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333978Generated: October 30, 2026
Triethylamine → 4-Chloro-N-methylpicolinamide
https://huagongshe.com/reaction/333978
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | 4-chloropyridine-2-carbonyl Chloride | HCID 11095146 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Chloro-N-methylpicolinamide | HCID 1476814 | 52.4% |
Reaction Steps
To a solution of methylamine hydrochloride (2.057 g, 30.5 mmol) and triethylamine (14.16 ml, 102 mmol) in DCM (30 ml) at 0° C., was added 4-chloropyridine-2-carbonyl chloride (3.575 g, 20.31 mmol) in DCM (20 ml). The resulting black suspension was allowed to reach room temperature and stirred overnight. The mixture was concentrated under reduced pressure and dissolved in ethyl acetate. Water was added and the layers were separated. The aqueous layer was extracted with ethyl acetate (3×), the combined organic layers were washed with water (3×) and brine, dried with Na2SO4 and concentrated under reduced pressure. The residue was purified with column chromatography (20-50% ethyl acetate in n-heptane) to give 2.04 gram of a yellow oil (10.64 mmol, 52%). MS (ESI) m/z=170.0 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883791B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-c01a2569c4454daeb1754f553090b0c5 |
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| Source note | uspto-grants-2014_11 |
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