HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 1-(4-Fluoro-phenyl)-1H-indazole-4-carboxylic acid (6-bromo-pyridin-3-ylmethyl)-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-bromo-N-methylpyridin-3-amine | HCID 817178 | — |
| Reactant | 1-(4-fluoro-phenyl)-1H-indazole-4-carboxylic acid chloride | HCID 58138874 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Fluoro-phenyl)-1H-indazole-4-carboxylic acid (6-bromo-pyridin-3-ylmethyl)-amide | HCID 44469661 | — |
Reaction Steps
A mixture of 1-(4-fluoro-phenyl)-1H-indazole-4-carboxylic acid chloride (416 mg, 1.51 mmol), 6-bromo-pyridin-3-yl-methylamine (311 mg, 1.66 mmol) and DMAP (18.5 mg, 0.151 mmol) in DCM (10 mL) was treated with DIEA (1.32 mL, 7.56 mmol). The solution was stirred at room temperature. After 16 hours the mixture was diluted with DCM (30 mL). The organic layer was washed with saturated aqueous NH4Cl (2×10 mL), saturated aqueous NaHCO3 (2×10 mL), water (10 mL), brine (10 mL) and dried over MgSO4, filtered and concentrated. The residue was purified by silica gel chromatography eluting with a gradient of 0-50% ethyl acetate in hexanes to afford the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08263597B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-ac3a6a00c17c4c2997d1578d672ecefe |
| Source note | uspto-grants-2012_09 |