Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | HCID 86595893 | HCID 86595893 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | HCID 69067026 | HCID 69067026 | 32.7% |
Reaction Steps
A mixture of 3-cyano-7-[(2R)-2,3-epoxypropoxy]-6-methoxy-4-(2,3-methylenedioxyanilino)quinoline (0.1 g), morpholine (0.11 g) and propanol (5 ml) was stirred and heated to 80° C. for 3 hours. The resultant mixture was evaporated and the residue was purified by column chromatography on silica using increasingly polar mixtures of methylene chloride and methanol as eluent. The material so obtained was triturated under diethyl ether to give the title compound (0.04 g); NMR Spectrum: (DMSOd6) 2.35-2.52 (m, 6H), 3.56 (m, 4H), 3.93 (s, 3H), 4.04.1 (m, 2H), 4.17 (m, 1H), 4.9 (d, 1H), 5.98 (s, 2), 6.9-6.92 (m, 3H), 7.33 (s, 1H), 7.86 (s, 1H), 8.4 (s, 1H), 9.48 (br s, 1H); Mass Spectrum: M−H− 477.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07501516B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-02299f06a64e41adb6ac5ef29d0c9252 |
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| Source note | uspto-grants-2009_03 |
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