Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminopyridine | HCID 1727 | — |
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | HCID 54710119 | HCID 54710119 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54712461 | HCID 54712461 | 67% |
Reaction Steps
A mixture of 2.48 g (10.4 mmols) of ethyl 4,5-dihydro-7-hydroxy-5-oxothieno[3,2-b]pyridine-6-carboxylate [J. Chem. Res. (S), 6 (1980); J. Chem. Res. (M), 113 (1980)], 1.01 g (10.7 mmols) of 4-aminopyridine, 50 ml of xylene and 10 ml of dimethylformamide was heated at 140° C. for an hour. After completion of the reaction, insoluble matters were filtered and tritylated with dimethylformamide with heating to give 1.99 g (yield: 67%) of Compound 2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05219864 |
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| Source dataset | uspto-grants-1993_06 |
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| ORD ID | ord-2c94fb6ae6784a99b485d1c0569d815f |
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| Source note | uspto-grants-1993_06 |
|---|