HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → (R)-5-(4-Cyanobenzyl)-7-(3,5-dichlorophenyl)-5-methyl-6-oxo-6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-carboxylic acid [1-acetyl-4-(1-pyridin-2-yl-cyclopropylcarbamoyl)-piperidin-4-yl]-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | (R)-5-(4-cyanobenzyl)-7-(3,5-dichlorophenyl)-5-methyl-6-oxo-6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-carboxylic acid [4-(1-pyridin-2-yl-cyclopropylcarbamoyl)-piperidin-4-yl]-amide | HCID 58431246 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | (R)-5-(4-Cyanobenzyl)-7-(3,5-dichlorophenyl)-5-methyl-6-oxo-6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-carboxylic acid [1-acetyl-4-(1-pyridin-2-yl-cyclopropylcarbamoyl)-piperidin-4-yl]-amide | HCID 42632964 | — |
Reaction Steps
To a solution of (R)-5-(4-cyanobenzyl)-7-(3,5-dichlorophenyl)-5-methyl-6-oxo-6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-carboxylic acid [4-(1-pyridin-2-yl-cyclopropylcarbamoyl)-piperidin-4-yl]-amide (20 mg, 0.03 mmol) in pyridine (0.5 mL) was added acetic anhydride (0.5 mL). The reaction mixture was stirred at room temperature for 1 h. The solvent was removed in vacuo and the remaining residue was dissolved in water and extracted with CH2Cl2 (3×10 mL). The organic layer was washed with brine and dried over Na2SO4. After removal of the solvent in vacuo, the title compound was obtained as a white solid (21 mg), m/z 725.5 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552205B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-21b87dabba084743b2e0328713d23290 |
| Source note | uspto-grants-2013_10 |