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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573543Generated: October 30, 2026

Dichloromethane → 3-(3-Chlorophenyl)-2,6-dimethylthieno[2,3-b]pyridin-4-amine

https://huagongshe.com/reaction/573543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantCesium carbonateHCID 10796—
Reactant(3-Chlorophenyl)boronic acidHCID 2734323—
Reactant3-Bromo-2,6-dimethylthieno[2,3-b]pyridin-4-amineHCID 68323862—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product3-(3-Chlorophenyl)-2,6-dimethylthieno[2,3-b]pyridin-4-amineHCID 68324017107.1%

Reaction Conditions

Temperature150 °C

Reaction Steps

Under nitrogen, 3-bromo-2,6-dimethylthieno[2,3-b]pyridin-4-amine (170 mg, 0.661 mmol) (Description 8) was dissolved in toluene (6 mL) and (3-chlorophenyl)boronic acid (155 mg, 0.992 mmol), PdCl2(dppf).DCM (54.0 mg, 0.066 mmol) and Cs2CO3 (646 mg, 1.983 mmol) were added and the mixture heated in a microwave at 150° C. for 30 min. The reaction mixture was combined with the material (30 mg) from similar reaction. Water (20 mL) was added and the mixture extracted with ethyl acetate (3×15 mL). The organic layer was dried over MgSO4, filtered and solvent removed in vacuo. Purification by chromatography on silica gel, eluting with a gradient of 0-50% ethyl acetate in cyclohexane, afforded the title compound (204.4 mg). LCMS (A) m/z: 291 [M+1]+, Rt 0.84 min (acidic).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029545B2
Source datasetuspto-grants-2015_05
ORD IDord-a16e56a030414cecbdba2da572508c5e
Source noteuspto-grants-2015_05