Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | 6-(4-Aminophenyl)-1,2-dihydro-2-oxonicotinic acid | HCID 12918956 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 20554253 | HCID 20554253 | — |
Reaction Steps
Methyl chloroformate, 1.7 ml (20 mM), was added to a solution of 2.9 g (20 mM) of alpha-acetamidoisobutyic acid, 2.2 ml (20 mM) of N-methylmorpholine in 50 ml CH3CN at -15° C. The mixture was stirred at -20° C. to -10° C. for 1/2 hr and to it was added in a dropwise manner preformed silylated pyridone solution (by stirring a mixture of 2.3 g (10 mM) of the 6-(4-aminophenyl)-1,2-dihydro-2-oxonicotinic acid, 3.84 ml (30 mM) of Me3SiCl, 4.2 ml (30 mM) of Et3N in 100 ml CH2Cl2 for 40 min) at -10° C. After the addition, the mixture was allowed to stir at 0° C. for 2 hrs and at room temperature for 12 hrs. To the resulting suspension was added 10 ml of isopropanol, stirred for 10 min, and the solids filtered, washed with MeOH, ether, dried to give 2.5 g of 6-[4-(N-acetyl-alpha-amino-isobutyrylamino)phenyl]-1,2-dihydro-2-oxonicotinic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04278681 |
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| Source dataset | uspto-grants-1981_07 |
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| ORD ID | ord-5b54233982004201b26855239acb785e |
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| Source note | uspto-grants-1981_07 |
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