Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | HCID 21266445 | HCID 21266445 | — |
| Reactant | HCID 21266528 | HCID 21266528 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 21266526 | HCID 21266526 | — |
Reaction Steps
Preparation of 4-(3-methylphenyl)-5-(4-pyridyl)-1H-pyrid-one To a solution of 6-hydroxy-4-m-tolyl-5,6-dihydro-1H-[5,4′]bipyridinyl-2-one (83 mg, 0.29 mmole) in CHCl3 (3 mL) at r.t. was added 2 ml of conc. H2SO4. The resulting mixture was heated to 55° C. for 2 hr. The mixture was cooled down to r.t. and was carefully quenched with aqueous sodium carbonate. Standard work up (extraction of compound with methylene chloride), followed by purification (silica gel, methanol/methylene chloride) gave the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06174901B1 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-156082663a234f08981c25041ef8ae6e |
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| Source note | uspto-grants-2001_01 |
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