HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 623949Generated: October 29, 2026
Methanamine, N-methoxy-, hydrochloride (1:1) → N-methoxy-N-methyl-6-(trifluoromethyl)nicotinamide
https://huagongshe.com/reaction/623949
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-(Trifluoromethyl)nicotinoyl chloride | HCID 2777557 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-methoxy-N-methyl-6-(trifluoromethyl)nicotinamide | HCID 23116945 | — |
Reaction Steps
To a 1 L 3-neck flask equipped with an overhead stirrer, Claisen adaptor, nitrogen bubbler, 125 mL addition funnel, and thermocouple was added 6-(trifluoromethyl)nicotinoyl chloride (49.3 g, 235 mmol, Intermediate 2, step a), dichloromethane (493 mL), and N,O-dimethylhydroxylamine hydrochloride (25.63 g, 258.8 mmol). After the mixture was cooled to 7° C., diisopropylethylamine (90.26 mL, 517.6 mmol) was added such that the addition temperature did not exceed 16° C. After the addition, the reaction was allowed to warm to room temperature. The reaction was then transferred to a separatory funnel and the organic layer was washed with saturated NaHCO3 (2×100 mL) followed by water (100 mL) and then dried over sodium sulfate and filtered. Solvent removal afforded a brownish oil as the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09303015B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-75bd22f57cf1417b83aae40e80675249 |
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| Source note | uspto-grants-2016_04 |
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