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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1175372Generated: October 31, 2026

p-Toluenesulfonic acid → HCID 11591385, compound

https://huagongshe.com/reaction/1175372

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantAnisoleHCID 7519—
ReactantHCID 67051259HCID 67051259—
SolventMethanolHCID 887—
ProductHCID 11591385HCID 11591385—

Reaction Steps

To a solution of N-[2-[[(2,3-difluorophenyl)methyl]thio]-6-[(1R)-1-methyl-2-(triphenylmethoxy)ethoxy]-4-pyrimidinyl]-1,6-dihydro-1-methyl-6-oxo-3-pyridinesulfonamide (the product from step ii) (0.16 g) in MeOH (10 mL) was added p-toluenesulfonic acid (50 mg) and anisole (0.22 g). The reaction was then stirred at room temperature for 18 h. The reaction was partitioned between EtOAc (100 mL) and H2O (100 mL). The aqueous layer was then further extracted with EtOAc (2×100 mL). Combined organic layers were dried (MgSO4), filtered and evaporated. The residue was purified by reverse phase HPLC using TFA (0.2%)/MeCN to give a white solid. Yield: 9 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07838675B2
Source datasetuspto-grants-2010_11
ORD IDord-eb7f4b304ab9479ba8c73575e97afab8
Source noteuspto-grants-2010_11