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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401316Generated: October 26, 2026

6-Bromo-3-pyridinecarboxaldehyde → 6-(7-(2-Fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)nicotinaldehyde

https://huagongshe.com/reaction/1401316

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-3-pyridinecarboxaldehydeHCID 11769234—
Reactant7-(2-Fluoro-4-nitrophenoxy)-2-iodothieno[3,2-b]pyridineHCID 59457661—
ReactantHCID 178477788HCID 178477788—
Solvent1,4-DioxaneHCID 31275—
Product6-(7-(2-Fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)nicotinaldehydeHCID 5945766650.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of intermediate 24 (6 g, 14.42 mmol) in dioxane (40 mL) were added 6-bromopyridine-3-carbaldehyde (7) (3.22 g, 17.30 mmol), palladium tetrakistriphenylphosphine (0.500 g, 0.433 mmol), and hexamethyldistannane (3.29 mL, 15.86 mmol). The mixture was heated at 100° C. for 20 h, concentrated, adsorbed on silica gel, placed onto a silica gel column and subjected to flash chromatography purification (eluent DCM/MeOH: 100/0, 99/1, 98/2, 97/3), to afford intermediate 25 (2.864 g, 50% yield). MS (m/z): 396.1 (M+H). N-((6-(7-(2-Fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)-2-methoxyethanamine (26)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907091B2
Source datasetuspto-grants-2014_12
ORD IDord-62edf402cdc34e8ab67006a198980e72
Source noteuspto-grants-2014_12