HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2185837Generated: October 31, 2026
N-Methylbenzylamine → HCID 22452596, compound
https://huagongshe.com/reaction/2185837
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylbenzylamine | HCID 7669 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 15541009 | HCID 15541009 | — |
| Product | HCID 22452596 | HCID 22452596 | 73% |
Reaction Steps
To 5-(2-methylsulfonylpyrimidin-4-yl)-2-oxo-6-(3-trifluoromethylphenyl)-1,2-dihydropyridine-3-carbonitrile (150 mg, 0.357 mmol) in a sealed tube was added (S)-∝-methylbenzylamine (150 mg) and the mixture heated under argon at 100° C. for 1 hour. The reaction was cooled and the oil dissolved in ethyl acetate (25 mL). The solution was washed 3 times with a pH 5.3 buffer solution of 10% citric acid/NaOH (15 mL). The ethyl acetate layer was dried over sodium sulfate concentrated and chromatographed on silica using 80% ethyl acetate/hexane to give 120 mg (73%) of the title compound as a solid. The solid was stirred in methanol/hexane (2 mL) for 1 hour, filtered, and dried 40° C. to give 105 mg of a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06403596B1 |
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| Source dataset | uspto-grants-2002_06 |
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| ORD ID | ord-3d5a1a1d25b747a4ade895f0cfc48f2b |
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| Source note | uspto-grants-2002_06 |
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