HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 245577Generated: October 30, 2026
Potassium Cyanide → HCID 67434460, compound
https://huagongshe.com/reaction/245577
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | 18-Crown-6 | HCID 28557 | — |
| Reactant | HCID 67433770 | HCID 67433770 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67434460 | HCID 67434460 | — |
Reaction Steps
To a stirred solution of (2R,4S,4aS)-rel-11-fluoro-2,4-dimethyl-8-(methylsulfonyl)-1,2,4,4a-tetrahydro-2′H,6H-spiro[1,4-oxazino[4,3-a][1,2]oxazolo[4,5-g]quinoline-5,5′-pyrimidine]-2′,4′,6′(1′H,3′H)-trione (Example 182, 1.0 g, 2.15 mmol) in DMF was added KCN (700 mg, 10.75 mmol) followed by 18-crown-6 (catalytic) and the mixture was heated at 85° C. for 12 hours. The reaction mixture was cooled to room temperature and precipitated with diethyl ether (repeated twice to remove complete DMF). The precipitate was dissolved in EtOAc (50 mL) and washed with water (2×10 mL), dried over anhydrous sodium sulfate and, filtered, concentrated. The residue was purified by ‘combiflash instrument’ to give product as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658641B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-ef71a7a0d4174fed8fd434c33e1a6a71 |
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| Source note | uspto-grants-2014_02 |
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