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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17197Generated: October 27, 2026

Acrylonitrile → (2E)-3-(4-amino-3-bromothieno[3,2-c]pyridin-7-yl)acrylonitrile

https://huagongshe.com/reaction/17197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcrylonitrileHCID 7855—
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylphosphineHCID 11776—
Reactant3-Bromo-7-iodothieno[3,2-C]pyridin-4-amineHCID 18450791—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Product(2E)-3-(4-amino-3-bromothieno[3,2-c]pyridin-7-yl)acrylonitrileHCID 1845063988.5%

Reaction Conditions

Temperature77 °C

Reaction Steps

To a solution of 3-bromo-7-iodothieno[3,2-c]pyridin-4-ylamine (430 mg, 1.21 mmol), triphenylphosphine (128 mg, 0.48 mmol) and sodium carbonate (257 mg, 2.42 mmol) in N,N-dimethylformamide (6 ml) was added acrylonitrile (0.32 ml, 4.84 mmol) followed by palladium(II) acetate (56 mg, 0.24 mmol). The reaction was heated at 77° C. for 18 hours under an atmosphere of nitrogen. The mixture was allowed to cool to ambient temperature and solvents were removed under reduced pressure. The residue was purified by flash chromatography on silica gel using ethyl acetate as the mobile phase to give the title compound (300 mg, 88%) as an off-white solid used directly in the following Suzuki coupling step. LCMS (Conditions g); Rt2.28; MS: MH+ 280.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737160B2
Source datasetuspto-grants-2010_06
ORD IDord-2592824e09444e4f8496d0a25ab758a3
Source noteuspto-grants-2010_06