HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 6-Chloro-N-methoxy-N-methylnicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanamine, N-methoxy-, hydrochloride (1:1) | HCID 81138 | — |
| Reactant | 6-Chloronicotinoyl Chloride | HCID 2782165 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Chloro-N-methoxy-N-methylnicotinamide | HCID 11435597 | — |
Reaction Steps
Into a 1000-mL round-bottom flask, was placed methoxy(methyl)amine hydrochloride (12 g, 123.02 mmol), triethylamine (40 g, 395.30 mmol). This was followed by the addition of a solution of 6-chloropyridine-3-carbonyl chloride (17.6 g, 100.00 mmol, Intermediate 37: step a) in dichloromethane (100 mL) dropwise with stirring. The resulting solution was stirred for 12 hours at room temperature. The solids were filtered out. The resulting mixture was concentrated under vacuum to give the title compound as yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09290476B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-b29320aea1814812861606fed300a499 |
| Source note | uspto-grants-2016_03 |