Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400897Generated: November 1, 2026

7-Chlorothieno[3,2-b]pyridine → 2-(6-(1,3-Dioxan-2-yl)pyridin-3-yl)-7-chlorothieno[3,2-b]pyridine

https://huagongshe.com/reaction/1400897

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Chlorothieno[3,2-b]pyridineHCID 11275251—
Reactant5-Bromo-2-(1,3-dioxan-2-yl)pyridineHCID 58474564—
ReactantButyllithiumHCID 178418339—
CatalystZincchlorideHCID 3007855—
SolventTetrahydrofuranHCID 8028—
Product2-(6-(1,3-Dioxan-2-yl)pyridin-3-yl)-7-chlorothieno[3,2-b]pyridineHCID 5847489259%

Reaction Steps

To a stirred solution of 7-chlorothieno[3,2-b]pyridine (12.08 g, 71.2 mmol) in THF (138 mL) at −15° C. was added n-BuLi (30.7 mL, 77.0 mmol). After 30 min, a solution of ZnCl2 0.5 M in THF (142 mL, 71.2 mmol) was added at −15° C. and the reaction mixture was allowed to warm to RT over 45 min. A solution of palladium tetrakistriphenylphosphine (1.266 g, 1.096 mmol) and bromide 278 (13.37 g, 54.8 mmol) in THF (18.5 mL) was added and the mixture was heated to reflux for 2 h then concentrated. The residue was diluted with water and ammonium hydroxide and extracted with DCM. The organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated. The residue was triturated with MTBE to afford the title compound 279 (10.70 g, 32.2 mmol, 59% yield) as light brown solid. MS (m/z): 333.33 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906852B2
Source datasetuspto-grants-2014_12
ORD IDord-d45fb2b9a1304b0fb4334e3338588d68
Source noteuspto-grants-2014_12