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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517826Generated: November 3, 2026

p-Toluenesulfonic acid → (S)-1-(4-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenylcarbamoyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydropyrazol-1-yl)propan-2-yl 2-(dimethylamino)acetate 4-methylbenzenesulfonate

https://huagongshe.com/reaction/1517826

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant(S)-1-(4-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenylcarbamoyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydropyrazol-1-yl)propan-2-yl 2-(dimethylamino)acetateHCID 59491008—
Product(S)-1-(4-(3-fluoro-4-(7-methoxyquinolin-4-yloxy)phenylcarbamoyl)-5-methyl-3-oxo-2-phenyl-2,3-dihydropyrazol-1-yl)propan-2-yl 2-(dimethylamino)acetate 4-methylbenzenesulfonateHCID 86645597—

Reaction Steps

The title compound was prepared according to the procedure described in Example 35 step 2 by using the compound of (S)-1-(4-(4-(7-methoxyquinolin-4-yloxy)-3-fluoro-phenylcarbamoyl)-2,3-dihydro-5-methyl-3-oxo-2-phenylpyrazol-1-yl)propan-2-yl 2-(dimethylamino)acetate (62.9 mg, 0.1 mmol) and p-toluene sulphonic acid (34.6 mg, 0.2 mmol, Shanghai chemical reagent factory). The desired compound was abtained as a yellow solid (56.1 mg, 57%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232294B2
Source datasetuspto-grants-2012_07
ORD IDord-8cc40c9f506d4b9c99cad632f31d7d26
Source noteuspto-grants-2012_07