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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645654Generated: October 27, 2026

(4-(5,9-Dioxaspiro[3.5]non-7-yloxy)pyridin-2-yl)methanol → HCID 66776211, compound

https://huagongshe.com/reaction/1645654

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-(5,9-Dioxaspiro[3.5]non-7-yloxy)pyridin-2-yl)methanolHCID 59792459—
ReactantHCID 66776433HCID 66776433—
ProductHCID 66776211HCID 66776211—

Reaction Steps

The same procedure as in the steps (9h) to (9j) of Example 9 was repeated using the (4-(5,9-dioxaspiro[3.5]non-7-yloxy)pyridin-2-yl)methanol obtained in the step (83b) above to obtain the title compound (100 mg, the total yield of 3 steps: 50%) as a white solid. Note that, in the same process as in the step (9h), 2-mercaptobenzimidazole was added to the reaction mixture and stirred at room temperature for 25 hours, and thereafter, 3 equivalents of potassium hydroxide relative to the alcohol was added thereto. The mixture was allowed to react at room temperature for 6 hours.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124780B2
Source datasetuspto-grants-2012_02
ORD IDord-1e992ff1e34f496fbd73ad93a55e7bc9
Source noteuspto-grants-2012_02