HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 50991461, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 50991733 | HCID 50991733 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 50991461 | HCID 50991461 | — |
Reaction Steps
Acetic anhydride (4.8 μL, 0.5.1 μmol) was added to a mixture solution of 3-(3-(4-(2-(dimethylamino)ethoxy)phenyl)-1-(pyridin-4-yl)-1H-indol-6-yl)benzenamine (2.2 mg, 4.9 μmol) in pyridine (0.4 mL) at room temperature. After stirring for 15 hours at room temperature, the reaction solution was added to saturated sodium bicarbonate aqueous solution and then extracted with ethyl acetate. The collected organic layer was washed with brine and concentrated under reduced pressure by drying with anhydrous magnesium sulfate. The residue was purified by chromatography (preparative TLC, DCM:MeOH=10:1). The target compound (1.5 mg) was obtained as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08648089B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-59e48ea1db524dd6b8233ccc5efc34aa |
| Source note | uspto-grants-2014_02 |