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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2384943Generated: November 2, 2026

N,N'-Dimethylethylenediamine → 2-(4-Chloro-phenyl)-6-[4-(1-methyl-pyrrolidine-3-carbonyl)-phenyl]-6h-thieno[2,3-c]pyridin-7-one, hydrochloride

https://huagongshe.com/reaction/2384943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-DimethylethylenediamineHCID 8070—
ReactantCesium carbonateHCID 10796—
ReactantEther hydrochlorideHCID 10953452—
Reactant2-(4-Chlorophenyl)-6H,7H-thieno[2,3-c]pyridin-7-oneHCID 57649519—
ReactantHCID 68951075HCID 68951075—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product2-(4-Chloro-phenyl)-6-[4-(1-methyl-pyrrolidine-3-carbonyl)-phenyl]-6h-thieno[2,3-c]pyridin-7-one, hydrochlorideHCID 24803746151.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

Combine 2-(4-chloro-phenyl)-6H-thieno[2,3-c]pyridin-7-one (0.15 g, 0.57 mmol), (4-bromo-phenyl)-(1-methyl-pyrrolidin-3-yl)-methanone (0.16 g, 0.60 mmol), Cs2CO3 (0.37 g, 1.15 mmol), 1,4-dioxane (6 mL), and CuI (0.044 g, 0.23 mmol). Purge the mixture with nitrogen for 10 min. Add sym-dimethylethylene diamine (0.040 g, 0.46 mmol). Heat the mixture at 100° C. overnight. Cool the mixture to RT, dilute with CH2Cl2 (200 mL), and wash with a solution of 5% NH4OH/H2O (2×30 mL). Dry the organic layer over Na2SO4, filter, and concentrate. Filter the crude with H2O (200 mL) and Et2O (100 mL). Prepare the HCl salt by dissolving the solid in CH2Cl2 and adding 1 eq 1M HCl/ether. Allow the solution to stir for 15 min and concentrate to give 0.21 g (77%) of the title compound. LC-MS/ES m/z (35Cl) 449.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263772B2
Source datasetuspto-grants-2012_09
ORD IDord-3ec9ae2f2d854c2fb27b702b4996fa66
Source noteuspto-grants-2012_09