Reaction #59914

ord-380c7708f36f419d9928cc628ccd408a

Reaction equation

COC1OCC(COc2ccnc(CS(=O)c3nc4ccccc4[nH]3)c2C)CO1.[Na]
( 6f )
COC1OCC(COc2ccnc(CS(=O)c3nc4ccccc4[nH]3)c2C)CO1.[Na]
2-(((4-((2-methoxy-1,3-dioxan-5-yl)methoxy)-3-methylpyridin-2-yl)methyl)sulfinyl)-1H-benzimidazole sodium salt
OC1CCC2(CC1)OCCO2
1,4-dioxaspiro[4.5]decan-8-ol
Cc1c(OC2CCC3(CC2)OCCO3)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
title compound
Yield 7.3%
Cc1c(OC2CCC3(CC2)OCCO3)ccnc1CS(=O)c1nc2ccccc2[nH]1.[Na]
2-(((4-(1,4-dioxaspiro[4.5]dec-8-yloxy)-3-methylpyridin-2-yl)methyl)sulfinyl)-1H-benzimidazole sodium salt
Yield 7.3%

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    Otherobtained in the step (27a)

Procedure

The same procedure as in the steps (6b) to (6f) of Example 6 was repeated using 1,4-dioxaspiro[4.5]decan-8-ol obtained in the step (27a) to obtain the title compound (230 mg, total yield: 7.3%) as a light yellow solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07425634B2uspto-grants-2008_09