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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270923Generated: October 31, 2026

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

https://huagongshe.com/reaction/1270923

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 numberUS07202363B2
Source datasetuspto-grants-2007_04
ORD IDord-37bcc1eaf05442c18bbde293ea394239
Source noteuspto-grants-2007_04