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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984670Generated: November 2, 2026

4-Ethynyl-5-methyl-3-phenyl-isoxazole → HCID 24784179, compound

https://huagongshe.com/reaction/1984670

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Ethynyl-5-methyl-3-phenyl-isoxazoleHCID 53434647—
ReactantHCID 68852842HCID 68852842—
ProductHCID 24784179HCID 2478417921%

Reaction Steps

As described for example 11c, 4-ethynyl-5-methyl-3-phenyl-isoxazole (92 mg, 0.50 mmol) was converted [using 2-iodo-5-methyl-1-phenyl-1H-imidazole (prepared from 5-methyl-1-phenyl-1H-imidazole by reaction of 4(5)-methyl-1-phenyl-1H-imidazole with N-iodosuccinimide in N,N-dimethylformamide at ambient temperature) instead of 2-chloro-4-iodopyridine] to the title compound (SiO2, heptane:ethyl acetate=95:5 to 0:100, 35 mg, 21%) which was obtained as a brown solid. MS: m/e=340.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544704B2
Source datasetuspto-grants-2009_06
ORD IDord-befc431f4d0d4d98ab3b36db5df1659f
Source noteuspto-grants-2009_06