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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508961Generated: October 31, 2026

2,4-Dichloro-6,7-dihydro-5H-cyclopenta[b]pyridine → HCID 90338558, compound

https://huagongshe.com/reaction/1508961

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-6,7-dihydro-5H-cyclopenta[b]pyridineHCID 12214817—
Reactant2-(Tri-n-butylstannyl)oxazoleHCID 15486183—
CatalystHCID 178418397HCID 178418397—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 90338558HCID 9033855834.1%

Reaction Conditions

Temperature110 °C

Reaction Steps

To a solution of 2,4-dichloro-6,7-dihydro-5H-cyclopenta[b]pyridine (0.152 g, 0.81 mmol) in dioxane (3 mL) was added 2-(tributylstannyl)oxazole (0.318 g, 0.89 mmol) and tetrakis(triphenylphosphine)palladium (0.046 g, 0.040 mmol). The mixture was purged with nitrogen and then heated to 110° C. under sealed conditions for 16 h. After this time, the mixture was diluted with water and extracted with ethyl acetate. The organic layer were dried over anhydrous sodium sulfate, filtered, and the filtrate was concentrated. The residue was purified by column chromatography (silica, hexanes/ethyl acetate) to afford the title compound (0.061 g, 34%) as a white solid. MW=220.66. 1H NMR (CDCl3, 500 MHz) δ 7.94 (s, 1H), 7.78 (s, 1H), 7.29 (s, 1H), 3.19 (t, J=7.5 Hz, 2H), 3.06 (t, J=7.5 Hz, 2H), 2.22 (quin, J=7.5 Hz, 2H); APCI MS m/z 221 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221843B2
Source datasetuspto-grants-2015_12
ORD IDord-6dac63e83635445498518a0c5ab6633c
Source noteuspto-grants-2015_12