Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-chloro-N-(4-methoxyphenyl)pyridine-3-carboxamide | HCID 1483269 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 62173193 | HCID 62173193 | 90% |
Reaction Steps
Methanol (20 mL), triethylamine (1.59 mL, 11.4 mmol) and monomethylamine (2.0 M in MeOH, 19 mL, 38.0 mmol) were added to a pressure tube containing 6-chloro-N-(4-methoxyphenyl)nicotinamide (37, 2.0 g, 7.61 mmol) obtained in step 1. After agitating at 100° C. overnight and then cooling to room temperature, the product was removed by filtration. Removal of the solvent under reduced pressure yielded the target compound 6-(N-monomethylamino)-N-(4-methoxyphenyl)nicotinamide (38, 1.76 g, 90%) without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09133143B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-5b145deb8da54794be45b23421a6f397 |
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| Source note | uspto-grants-2015_09 |
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