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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2388756Generated: November 2, 2026

p-Toluenesulfonic acid → HCID 11591385, compound

https://huagongshe.com/reaction/2388756

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 numberUS08269002B2
Source datasetuspto-grants-2012_09
ORD IDord-083d4a42864742ac832c8e6af745d35c
Source noteuspto-grants-2012_09