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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371590Generated: November 1, 2026

p-Toluenesulfonic acid monohydrate → HCID 11975201, compound

https://huagongshe.com/reaction/1371590

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant4-(4-Methylpiperazin-1-yl)anilineHCID 737253—
Reactant(4-amino-2-ethanesulfonyl-pyrimidin-5-yl)-(3-fluoro-phenyl)-methanoneHCID 11974951—
SolventIsopropanolHCID 3776—
ProductHCID 11975201HCID 1197520168%

Reaction Conditions

Temperature105 °C

Reaction Steps

A suspension of (4-amino-2-ethanesulfonyl-pyrimidin-5-yl)-(3-fluoro-phenyl)-methanone (20.1 mg, 0.0650 mmol, Example 3), 4-(4-methylpiperazino)aniline (15.8 mg, 0.0826 mmol, Appolo Chemical) and p-toluenesulfonic acid hydrate (15 mg, 0.0777 mmol, Aldrich) in isopropanol (2.5 mL) was placed in a sealed tube and heated at 100 to 110° C. under microwave conditions for 1 hour. The resulting mixture was evaporated in vacuo and the crude product was purified on silica gel with 95:5 of dichloromethane/methanol to give [4-amino-2-[4-(4-methyl-piperazin-1-yl)-phenylamino]-pyrimidin-5-yl]-(3-fluoro-phenyl)-methanone as a light yellow solid (16.4 mg, 68% yield). HRMS, observed: 407.1994; Calcd for (M+H)+: 407.1990.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157455B2
Source datasetuspto-grants-2007_01
ORD IDord-90071b51cb784a74b273e9b0244350dd
Source noteuspto-grants-2007_01