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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040865Generated: November 1, 2026

3-(Phenylethynyl)-1-oxa-2,8-diazaspiro[4.5]dec-2-ene → 3-[(6-Methylpyridin-2-yl)ethynyl]-1-oxa-2,7-diazaspiro[4.4]non-2-ene

https://huagongshe.com/reaction/2040865

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Phenylethynyl)-1-oxa-2,8-diazaspiro[4.5]dec-2-eneHCID 57493808—
Reactanttert-Butyl 3-[(6-methylpyridin-2-yl)ethynyl]-1-oxa-2,7-diazaspiro[4.4]non-2-ene-7-carboxylateHCID 57493833—
SolventChloroformHCID 6212—
Product3-[(6-Methylpyridin-2-yl)ethynyl]-1-oxa-2,7-diazaspiro[4.4]non-2-eneHCID 5749383494.5%

Reaction Steps

The title compound was synthesized following the method reported for the Compound 1c, substituting Compound 1b with Compound 35a and running the reaction in chloroform. The crude brownish oily residue was used without further purification in the next reaction step. Yield: 94.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580962B2
Source datasetuspto-grants-2013_11
ORD IDord-2db1f32d642542758012f1937ce7446e
Source noteuspto-grants-2013_11