Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | HCID 53669110 | HCID 53669110 | — |
| Product | HCID 53888460 | HCID 53888460 | — |
Reaction Steps
2-Chloro-6-(4-fluorophenyl)-5-[4-(methylsulfonyl)phenyl]pyridine-3-carbonitrile (Example 7) (200 mg, 0.52 mMol) was charged with methylamine. The solution was shaken for 24 hours at 70° C. and 74 psi by a Parr Shaker. The vessel was cooled to room temperature and vented to allow excess methylamine to evaporate leaving a yellow solid. The solid was washed with methyl alcohol and recrystallized from chloroform: m.p. (DSC): 295.63° C. Anal. Calc'd. for C20H16N3O2SF (381.43): C, 62.98; H, 4.23; N, 11.02. Found: C, 62.59; H, 4.15; N, 10.77.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05686470 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-ea8afbef41dd4bdd9937b234cde26341 |
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| Source note | uspto-grants-1997_11 |
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