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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400861Generated: November 3, 2026

7-Chloro-2-(tributylstannyl)thieno[3,2-b]pyridine → 3-((6-(7-Chlorothieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)-1,3-oxazinan-2-one

https://huagongshe.com/reaction/1400861

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Chloro-2-(tributylstannyl)thieno[3,2-b]pyridineHCID 57516658—
ReactantHCID 58474481HCID 58474481—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product3-((6-(7-Chlorothieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)-1,3-oxazinan-2-oneHCID 5847463573.3%

Reaction Steps

To a solution of 197 (373 mg, 1.376 mmol) in toluene (10 mL) was added the 7-chloro-2-(tributylstannyl)thieno[3,2-b]pyridine 198 (631 mg, 1.376 mmol) and Pd(PPh3)4 (159 mg, 0.138 mmol). The reaction mixture was heated to reflux for 24 hours. The reaction mixture was then cooled to RT and concentrated. The residue was triturated with Et2O to afford the title compound 199 (363 mg, 73% yield) as beige solid. MS: 360 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906852B2
Source datasetuspto-grants-2014_12
ORD IDord-6626f45057c8456c99545eef386c5cff
Source noteuspto-grants-2014_12