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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729614Generated: October 30, 2026

Cyclopropanecarboxylic acid → Cyclopropyl-[4-(4-nitro-isoquinolin-1-yl)-piperazin-1-yl]-methanone

https://huagongshe.com/reaction/729614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopropanecarboxylic acidHCID 15655—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant4-Nitro-1-piperazin-1-yl-isoquinolineHCID 57832807—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductCyclopropyl-[4-(4-nitro-isoquinolin-1-yl)-piperazin-1-yl]-methanoneHCID 5783281679%

Reaction Steps

Treat a solution or slurry of 4-nitro-1-piperazin-1-yl-isoquinoline (Preparation 26, 517 mg, 2 mmol), cyclopropanecarboxylic acid (258 mg, 3 mmol) and catalytic DMAP (24 mg, 0.2 mmol) in dichloromethane (20 mL) with EDCI (575 mg, 3 mmol). Agitate the resulting mixture at ambient temperature overnight, then wash with saturated aqueous sodium bicarbonate solution. Dry the organic layer over sodium sulfate and concentrate under reduced pressure. Subject residue to silica gel chromatography using a gradient of 0-2% 2M ammonia-methanol in dichloromethane and a gradient of 0-70% ethyl acetate in hexanes to give a yellow solid after two purifications. (513 mg, 79% yield, LCMS ES+ (m/z) 327 [M+H]).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582638B2
Source datasetuspto-grants-2009_09
ORD IDord-fa1cd912677440fb9bb9a1bfb6c4050e
Source noteuspto-grants-2009_09