HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351856Generated: November 1, 2026
Potassium Hydroxide → HCID 136364557, compound
https://huagongshe.com/reaction/2351856
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 136364558 | HCID 136364558 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 136364557 | HCID 136364557 | — |
Reaction Steps
In an argon stream, 5 ml of ethanol was added to 175 mg (0.329 mM) of (-)-ethyl 3-[2-((S)-alpha-methoxybenzylcarbonyloxy)ethyl]-6-methyl-4-(3-nitrophenyl)-4,7-dihydroisothiazolo[5,4-b]pyridine-5-carboxylate obtained in Example 55 to form a solution. While the solution was cooled with ice-sodium chloride, 7 ml of a 7% aqueous solution of potassium hydroxide was added, and the mixture was stirred at the above temperature for 5 minutes. The reaction mixture was extracted with ethyl acetate. The ethyl acetate layer was washed successively with a saturated aqueous solution of sodium hydrogen carbonate, water and a saturated aqueous solution of sodium chloride, and then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to give (-)-ethyl 3-(2-hydroxyethyl)-6-methyl-4-(3-nitrophenyl)-4,7-dihydroisothiazolo[5,4-b]pyridine-5-carboxylate quantitatively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04874760 |
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| Source dataset | uspto-grants-1989_10 |
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| ORD ID | ord-719e02fd79444de195355e9dab0de138 |
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| Source note | uspto-grants-1989_10 |
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