HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881329Generated: November 1, 2026
Triethylamine → 6-Chloro-N-methoxy-N-methylnicotinamide
https://huagongshe.com/reaction/1881329
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N,O-Dimethylhydroxylamine | HCID 14232 | — |
| Reactant | 6-Chloronicotinoyl Chloride | HCID 2782165 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Chloro-N-methoxy-N-methylnicotinamide | HCID 11435597 | 89% |
Reaction Steps
A suspension of 2.3 g (12.81 mmol) of 6-chloronicotinoyl chloride and 1.53 g (15.37 mmol) of N,O-dimethylhydroxylamine in 46 mL of dichloromethane was cooled to 0° C. After dropwise addition of 5.36 mL (38.4 mmol) of triethylamine the resulting reaction mixture was warmed to RT and stirred for further 16 h. The mixture was subsequently washed with water (40 mL), 5% citric acid (40 mL), water (40 mL), and brine (40 mL). The organic layer was dried with Na2SO4, filtered, and the solvent was evaporated at reduced pressure yielding the titled compound as an oil. Amount 2.30 g. Yield 89%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08318793B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-5cbd430e48d64b6498ec7699c7f78625 |
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| Source note | uspto-grants-2012_11 |
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