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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428500Generated: November 2, 2026

Acetonitrile → 1'-(2,3-Dichloropyridin-4-yl)spiro[1-benzofuran-3,4'-piperidine]

https://huagongshe.com/reaction/1428500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
Reactant2,3-Dichloro-4-iodopyridineHCID 44887038—
Product1'-(2,3-Dichloropyridin-4-yl)spiro[1-benzofuran-3,4'-piperidine]HCID 86667987—

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of intermediate D10 (3 g, 10.953 mmol), 4-spiro-[3-(2,3-dihydro-benzofuran)]piperidine [CAS 171-77-7] (2.28 g, 12.049 mmoland DIPEA (7.63 ml, 43.814 mmol) in CH3CN (100 ml) was heated in a sealed tube at 110° C. for 3 days. The mixture was then treated with NaHCO3 (aqueous sat. solution) and extracted with EtOAc. The organic layer was separated, dried (Na2SO4) and concentrated in vacuo. The crude product was purified by column chromatography (silica gel; DCM/7M solution of NH3 in MeOH up to 4% as eluent), the desired fractions were collected and concentrated in vacuo to yield intermediate D48 (2.9 g, 63%) as a white solid. M.P. 177.2° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937060B2
Source datasetuspto-grants-2015_01
ORD IDord-5c9876c5627f43cfbcdce69dbe252246
Source noteuspto-grants-2015_01