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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852661Generated: October 31, 2026

N,N'-Dimethylethylenediamine → HCID 69359054, compound

https://huagongshe.com/reaction/852661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-DimethylethylenediamineHCID 8070—
Reactant2-PiperidoneHCID 12665—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantEthyl 3-ethyl-7-iodo-1H-indole-5-carboxylateHCID 69357900—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTolueneHCID 1140—
ProductHCID 69359054HCID 6935905427.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of ethyl 3-ethyl-7-iodo-1H-indole-5-carboxylate (D190) (1 g, 2.91 mmol, 1 equiv) in toluene (10 ml) were added 2-piperidinone (346 mg, 3.50 mmol, 1.2 equiv), K3PO4 (1.24 g, 5.83 mmol, 2 equiv), CuI (56 mg, 0.29 mmol, 0.1 equiv) and dimethyl ethylene diamine (62 μl, 0.58 mmol, 0.2 equiv) and the resulting mixture was stirred at 100° C. for 15 h then cooled to room temperature and concentrated in vacuo. The residue was partitioned between AcOEt and H2O and the layers were separated. The organic phase was dried under MgSO4 and concentrated in vacuo. Purification of the residue by flash chromatography on silica gel (AcOEt/iso-hexane: 1/0) gave ethyl 3-ethyl-7-(2-oxo-1-piperidinyl)-1H-indole-5-carboxylate (B165) (250 mg, 27%) as an off-white solid. [M+H]+=315.4, RT=2.98 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253198B2
Source datasetuspto-grants-2007_08
ORD IDord-f1325bdc72c44df9875ac3704089edd5
Source noteuspto-grants-2007_08