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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573597Generated: October 30, 2026

Dimethylformamide → 4-Amino-2,6-dimethylthieno[2,3-b]pyridine-3-carbonitrile

https://huagongshe.com/reaction/573597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantEthyl AcetateHCID 8857—
Reactant3-Bromo-2,6-dimethylthieno[2,3-b]pyridin-4-amineHCID 68323862—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystHCID 178418397HCID 178418397—
Product4-Amino-2,6-dimethylthieno[2,3-b]pyridine-3-carbonitrileHCID 68324063—

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 3-bromo-2,6-dimethylthieno[2,3-b]pyridin-4-amine (Description 8) (200 mg, 0.778 mmol), zinc cyanide (183 mg, 1.556 mmol) and tetrakis(triphenylphosphine)palladium(0) (90 mg, 0.078 mmol) in DMF (5 mL) was heated in a microwave at 140° C. for 1 h. Another batch of 3-bromo-2,6-dimethylthieno[2,3-b]pyridin-4-amine (200 mg, 0.778 mmol) was subjected to the same conditions. The mixtures were then combined and ethyl acetate (50 mL) added. The resulting mixture was washed with saturated NaHCO3 (20 mL) followed by brine (20 mL×2) and the organic layer dried over MgSO4, filtered and the solvent removed in vacuo. The residue was purified by normal phase chromatography, eluting with a gradient of 0-40% ethyl acetate in cyclohexane, to give the title compound (237.7 mg). LCMS (A) m/z: 204 [M+1]+, Rt 0.61 min (acidic).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029545B2
Source datasetuspto-grants-2015_05
ORD IDord-98aff5cbfb6845c4ae9ffd24de81a059
Source noteuspto-grants-2015_05