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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376161Generated: October 30, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 5-chloro-N-[1-(cyanomethyl)-2-oxo-1,2,3,4-tetrahydroquinolin-3-yl]-1H-indole-2-carboxamide

https://huagongshe.com/reaction/1376161

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Chloro-1H-indole-2-carboxylic acidHCID 82693—
Reactant(3-amino-2-oxo-3,4-dihydroquinolin-1(2H)-yl)acetonitrileHCID 21906832—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product5-chloro-N-[1-(cyanomethyl)-2-oxo-1,2,3,4-tetrahydroquinolin-3-yl]-1H-indole-2-carboxamideHCID 1004524278%

Reaction Steps

HOBT (168 mg, 1.24 mmol), 5-chloroindole-2-carboxylic acid (243 mg, 1.24 mmol), DIPEA (0.22 mL, 1.24 mmol) and then EDCI (296 mg, 1.55 mmol) were added to a solution of (3-amino-2-oxo-3,4-dihydroquinolin-1(2H)-yl)acetonitrile (Method 12, 250 mg, 1.24 mmol) in DCM (10 mL). The reaction was stirred for 18 h at ambient temperature, diluted with EtOAc (15 mL), washed with 1 N NaOH (15 mL), 1 N HCl (15 mL), saturated aqueous NaHCO3 solution (15 mL), dried (MgSO4) and the volatiles removed under reduced pressure to give the title compound (366 mg, 78%) as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169927B2
Source datasetuspto-grants-2007_01
ORD IDord-3ad868c3cfcc466b825a720c35ad06ba
Source noteuspto-grants-2007_01