HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 59170702, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium chloride monohydrate | HCID 57429219 | — |
| Reactant | HCID 59170865 | HCID 59170865 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 59170702 | HCID 59170702 | — |
Reaction Steps
To a THF (0.5 mL) solution of (E)-3-(3-formyl-4-(1H-imidazol-1-yl)phenyl)-N-indan-1-ylacrylamide (23 mg) obtained in Example 437, methyl magnesium bromide (3M ether solution, 0.04 mL) was added under nitrogen atmosphere under ice-cooling and the reaction mixture was agitated for 1 hour. A saturated ammonium chloride water and ethyl acetate were added to the reaction solution, and the organic layer was partitioned. The organic layer was washed with a saturated saline solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (Carrier: Chromatorex™ NH, elution solvent: methanol-ethyl acetate system), and 10 mg of the title compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07880009B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-eed56d7353f84c11a79aba3697cddf8f |
| Source note | uspto-grants-2011_02 |