HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → N-Cyclopropyl-3-fluoro-4-methyl-5-[1-(tetrahydro-2H-pyran-2-ylmethyl)-1H-indazol-5-yl]benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-(Bromomethyl)tetrahydro-2H-pyran | HCID 141917 | — |
| Reactant | N-Cyclopropyl-3-fluoro-5-(1H-indazol-5-yl)-4-methylbenzamide | HCID 10403067 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Chloroform ethylacetate | HCID 21584013 | — |
| Product | N-Cyclopropyl-3-fluoro-4-methyl-5-[1-(tetrahydro-2H-pyran-2-ylmethyl)-1H-indazol-5-yl]benzamide | HCID 11292707 | — |
Reaction Steps
Sodium hydride (60% in mineral oil, 12 mg) was added to N-cyclopropyl-3-fluoro-5-(1H-indazol-5-yl)-4-methylbenzamide (Intermediate 3, 45 mg) in DMF (5 ml) and the mixture was stirred at room temperature for 1 h. 2-(Bromomethyl)tetrahydro-2H-pyran (20.5 μl) was added and stirring continued for 18 h. The mixture was diluted with chloroform/ethyl acetate (1:1, 5 ml) and washed with water (2×5 ml). The organic phase was concentrated under vacuum and the residue was purified by preparative HPLC to give the title compound as a colourless glass (23 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07687532B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-1229b14028bb485c805ddc8e30b838cf |
| Source note | uspto-grants-2010_03 |