HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → Methyl 4-chloro-3'-((2-cyclopentyl-1-oxoisoindolin-5-yloxy)methyl)biphenyl-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Cyclopentyl-5-hydroxyisoindolin-1-one | HCID 50993654 | — |
| Reactant | Methyl 3'-(bromomethyl)-4-chlorobiphenyl-3-carboxylate | HCID 50994825 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | Methyl 4-chloro-3'-((2-cyclopentyl-1-oxoisoindolin-5-yloxy)methyl)biphenyl-3-carboxylate | HCID 50993811 | — |
Reaction Steps
To a solution of 2-cyclopentyl-5-hydroxyisoindolin-1-one (50 mg, 0.23 mmol) in acetone (15 mL), K2CO3 (181 mg, 1.31 mmol) was added methyl 3′-(bromo-methyl)-4-chlorobiphenyl-3-carboxylate (92 mg, 0.27 mmol) and the mixture was heated at reflux for 1 h. The reaction mixture was filtered and the solvent was evaporated in vacuo to obtain methyl 4-chloro-3′-((2-cyclopentyl-1-oxoisoindolin-5-yloxy)methyl)biphenyl-3-carboxylate as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08748632B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-15191c0d6e134eacb166e0a12fb8e4ca |
| Source note | uspto-grants-2014_06 |