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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278308Generated: October 30, 2026

Dimethylformamide → 2-(7-methylspiro[2H-benzofuran-3,1'-cyclopropane]-4-yl)oxy-5-nitro-pyridine

https://huagongshe.com/reaction/2278308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2-Chloro-5-nitropyridineHCID 78308—
Reactant7-methylspiro[2H-benzofuran-3,1-cyclopropane]-4-olHCID 57411301—
Product2-(7-methylspiro[2H-benzofuran-3,1'-cyclopropane]-4-yl)oxy-5-nitro-pyridineHCID 6796012690.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 7-methylspiro[2H-benzofuran-3,1′-cyclopropane]-4-ol (Intermediate 13, 176 mg, 1 mmol) in dry DMF (4 ml) potassium carbonate (207 mg, 1.5 mmol) and then 2-chloro-5-nitropyridine (158 mg, 1 mmol) were added and the reaction mixture was stirred for 2 hours at 80° C. After cooling the reaction mixture was quenched with water (2 ml), diluted with brine (10 ml) and extracted with ethyl acetate (2×20 ml). The organic layer was dried over sodium sulfate, filtered and evaporated affording the title compound (270 mg) as an orange solid that was used in the next step as crude material without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133175B2
Source datasetuspto-grants-2015_09
ORD IDord-8c697b400c794182bfe6ec9634a8b350
Source noteuspto-grants-2015_09