HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 50991639, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 50991638 | HCID 50991638 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 50991639 | HCID 50991639 | 90% |
Reaction Steps
Boron tribromide (BBr3, 17 μL, 0.182 mmol) was added to a mixture solution of 3-(4-methoxyphenyl)-6-(piperazin-1-yl)-1-(pyridin-4-yl)-1H-indole (14 mg, 0.036 mmol) in methylene chloride (0.5 mL) at −78° C. After stirring at room temperature for 15 hours, the reaction solution was added to a mixture solution of saturated sodium bicarbonate aqueous solution and ethyl acetate 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 target compound (12 mg) was obtained as yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08648089B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-1bee252900cd4fb2b5ce5e5b3ad31a61 |
| Source note | uspto-grants-2014_02 |