Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3-Furanol, tetrahydro- | HCID 9960 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 57799490 | HCID 57799490 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57799541 | HCID 57799541 | — |
Reaction Steps
NaH (70 mg) was carefully added to a solution of tetrahydro-furan-3-ol (0.2 ml) in DMF (3 ml) and the mixture was stirred for 1 hour. [1-Chloro-6-fluoro-7-(2-methoxy-ethoxy)-isoquinolin-3-yl]-(5-methyl-1H-pyrazol-3-yl)-amine (100 mg) was added under N2, and the mixture was heated at 90° C. overnight. The mixture was poured to 50 ml of water. The mixture was extracted by ethyl acetate (50 ml×3). The organic layer was evaporated to give [1-Chloro-7-(2-methoxy-ethoxy)-6-(tetrahydro-furan-3-yloxy)-isoquinolin-3-yl]-(5-methyl-1H-pyrazol-3-yl)-amine as oil (100 mg). LC-MS: m/e 419(MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07572809B2 |
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| Source dataset | uspto-grants-2009_08 |
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| ORD ID | ord-d17a7890e9d04341ac539aecbd9edc8e |
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| Source note | uspto-grants-2009_08 |
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