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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642739Generated: October 30, 2026

2-Aminoquinoline → (1S,3R)-[3-(quinolin-2-ylcarbamoyl)-cyclopentyl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1642739

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminoquinolineHCID 11379—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant(1S,3R)-3-(((tert-butoxy)carbonyl)amino)cyclopentane-1-carboxylic acidHCID 1512529—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product(1S,3R)-[3-(quinolin-2-ylcarbamoyl)-cyclopentyl]-carbamic acid tert-butyl esterHCID 66756862—

Reaction Steps

To a solution of Example 191A (91.6 mg, 0.4 mmol) in DMF (4 ml) was added 2-aminoquinoline (64 mg, 0.44 mmol), EDAC (93 mg, 0.48 mmol), HOBT (82 mg, 0.6 mmol), and diisopropylethylamine (0.35 ml, 2 mmol). The mixture was stirred at room temperature overnight, diluted with ethyl acetate, washed with water (2 times) and brine. The organic layer was dried (sodium sulfate), filtered, concentrated under reduced pressure and purified by flash chromatography with 3% methanol/dichloromethane to provide the titled compound. MS (ESI) m/z 356 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119664B2
Source datasetuspto-grants-2012_02
ORD IDord-d7e5bff7f2674528ab5c7dbdb9c56eaf
Source noteuspto-grants-2012_02