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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645643Generated: October 29, 2026

m-Chloroperbenzoic acid → 2-(((4-(2-(9-Methyl-1,5,8,10-tetraoxaspiro[5.5]undec-9-yl)ethoxy)pyridin-2-yl)methyl)sulfinyl)-1h-benzimidazole sodium salt

https://huagongshe.com/reaction/1645643

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-(9-Methyl-1,5,8,10-tetraoxaspiro[5.5]undec-9-yl)ethanolHCID 59792508—
Reactant2-(((3-Methyl-4-((8-methyl-1,4,7,9-tetraoxaspiro[4.5]dec-8-yl)methoxy)pyridin-2-yl)methyl)sulfinyl)-1h-benzimidazole sodium saltHCID 66776550—
Product2-(((4-(2-(9-Methyl-1,5,8,10-tetraoxaspiro[5.5]undec-9-yl)ethoxy)pyridin-2-yl)methyl)sulfinyl)-1h-benzimidazole sodium saltHCID 6677626511.4%

Reaction Steps

The same procedure as in the steps (5d) to (5h) of Example 5 (a reprecipitation operation was not performed in oxidation step with 3-chloroperbenzoic acid) was repeated using 2-(9-methyl-1,5,8,10-tetraoxaspiro[5.5]undec-9-yl)ethanol obtained in the step (76d) above to obtain the title compound (228 mg, total 11.4% yield) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124780B2
Source datasetuspto-grants-2012_02
ORD IDord-1d80a0f853494b69afb162bbe75e80c3
Source noteuspto-grants-2012_02