Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,6-Xylyl isothiocyanate | HCID 87976 | — |
| Reactant | 4-amino-6-methoxy-7-(N-methylpiperidin-4-ylmethoxy)quinazoline | HCID 22243908 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 9804543 | HCID 9804543 | 48.5% |
Reaction Steps
A solution of 4-amino-6-methoxy-7-(1-methylpiperidin-4-ylmethoxy)quinazoline (150 mg) in DMF (4.5 ml) was added to sodium hydride (60% dispersion in mineral oil, 0.03 g) and the reaction mixture was stirred at ambient temperature for 20 minutes. 2,6-Dimethylphenyl isothiocyanate (0.162 g) was added and the mixture was stirred at ambient temperature for 20 hours. The reaction mixture was evaporated and the residual solid-was purified by column chromatography on silica using increasingly polar mixtures of methylene chloride and a 2M solution of ammonia in methanol as eluent. There was thus obtained the title compound (0.112 g); NM Spectrum: (CDCl3) 1.44-1.61 (m, 2H), 1.87-2.08 (m, 5H), 2.32 (s, 3H), 2.36 (s, 6H), 2.94 (d, 2H), 4.04 (m, 5H), 7.1 (s, 1H), 7.19 (m, 3H), 7.29 (s, 1H), 8.69 (s, 1H), 8.9 (s, 1H), 13.37 (s, 1H); Mass Spectrum: M+H+ 466.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07498335B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-02e849ec93334d6dbdb5ddfd59d5f96a |
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| Source note | uspto-grants-2009_03 |
|---|