Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 18670248 | HCID 18670248 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18670596 | HCID 18670596 | — |
Reaction Steps
To a solution of 177 mg of 1-(10-methoxymethyl-10H-pyrazino[2,3-b][1,4]benzothiazin-8-ylmethyl)imidazol-2-carbaldehyde in a mixture of tetrahydrofuran (10 ml) with ethanol (10 ml) were added 0.5 ml of an aqueous solution of 0.24 g of silver nitrate and 1.5 N sodium hydroxide (4 ml) and the resulting mixture was stirred at room temperature for 15 hours. After filtering off the insoluble matters, the solution was concentrated under reduced pressure and the crystals of 1-(10-methoxymethyl-10H-pyrazino[2,3-b][1,4]benzothiazin-8-ylmethyl)imidazol-2-carboxylic acid thus precipitated were taken up by filtration. Next, the crystals were treated by the same method as the one of Example 9 to thereby give 55 mg of the title compound as orange crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06518423B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-bc9b806a528542038126b129df3c73c8 |
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| Source note | uspto-grants-2003_02 |
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