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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acrylonitrile | HCID 7855 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-Bromo-7-iodothieno[3,2-C]pyridin-4-amine | HCID 18450791 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (2E)-3-(4-amino-3-bromothieno[3,2-c]pyridin-7-yl)acrylonitrile | HCID 18450639 | 88.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07737160B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-2592824e09444e4f8496d0a25ab758a3 |
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| Source note | uspto-grants-2010_06 |
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