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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040553Generated: November 3, 2026

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

https://huagongshe.com/reaction/1040553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 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]-amideHCID 58431246—
SolventPyridineHCID 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]-amideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552205B2
Source datasetuspto-grants-2013_10
ORD IDord-21b87dabba084743b2e0328713d23290
Source noteuspto-grants-2013_10