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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182849Generated: October 26, 2026

Sodium Bicarbonate → (4-{2-[3-Methyl-4-(2,2,2-trifluoro-ethoxy)-pyridin-2-ylmethanesulfinyl]-benzimidazole-1-sulfonyl}phenoxy)acetic Acid 2-(toluene-4-sulfonyl)ethyl Ester

https://huagongshe.com/reaction/2182849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 20786417HCID 20786417—
SolventOxolane--water (1/1)HCID 21881883—
Product(4-{2-[3-Methyl-4-(2,2,2-trifluoro-ethoxy)-pyridin-2-ylmethanesulfinyl]-benzimidazole-1-sulfonyl}phenoxy)acetic Acid 2-(toluene-4-sulfonyl)ethyl EsterHCID 2078642372%

Reaction Steps

A solution of (3,5-dimethyl-4-{2-[3-methyl-4-(2,2,2-trifluoro-ethoxy)-pyridin-2-ylmethanesulfinyl]-benzimidazole-1-sulfonyl}phenoxy)acetic acid 2-(toluene-4-sulfonyl)ethyl ester (Intermediate 14, 400 mg, 0.50 mmol) and NaHCO3 (51 mg, 0.60 mmol, 1.2 eq) in THF-H2O (6 mL-3 mL) was heated to 70° C. for 3 h. Then volatile materials were removed, the residual gummy oil was dissolved in THF and the mixture was filtered to remove un-dissolved solid. The filtrate was dried, the solvent was removed by evaporation to give a yellow foam which was treated with ether-EtOAc (5:1) to precipitate a solid. The solid was treated with CH3CN, and then collected by filtration to give Compound 5 (230 mg, 72%) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897227B2
Source datasetuspto-grants-2005_05
ORD IDord-fcbf0a5be5e44cf48ebe6fef213d1516
Source noteuspto-grants-2005_05