Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Phosphinic Acid | HCID 4124402 | — |
| Reactant | HCID 18632325 | HCID 18632325 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Phosphoric Acid | HCID 1004 | — |
| Product | HCID 14552443 | HCID 14552443 | 100.1% |
Reaction Steps
A solution of 0.5 g (1.5 mmole) of ethyl 2-amino-5-propyl-trans-4,4a,5,6,8a,9-hexahydrothiazolo-[4,5-g]quinoline-7-carboxylate (Example 3) in 50 ml of 85% phosphoric acid was cooled to 0° C. Then 110 mg (1.8 mmole) of sodium nitrite dissolved in as small an amount of water as possible was slowly adeed under the surface of the reaction mixture. The resulting mixture was added dropwise to 50 ml of 50% hypophosphorous acid (H3PO2) at 0° C. The mixture was stirred at room temperature until gas evolution ceased. This took about 1 hour. The mixture was poured onto ice, and the hydrogen ion concentration of the mixture was adjusted to pH 11. Water was added to dissolve the preoipitate that formed; then the product was extracted into a solution of CHCl3 /i-PrOH (3:1). This solution was dried using sodium sulfate and evaporated to give 0.46 g of the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05134143 |
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| Source dataset | uspto-grants-1992_07 |
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| ORD ID | ord-1945b9d9c1974866b575351e78f5885b |
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| Source note | uspto-grants-1992_07 |
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