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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243184Generated: November 3, 2026

P-Anisidine → HCID 178492150, compound

https://huagongshe.com/reaction/1243184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP-AnisidineHCID 7732—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
ReactantHCID 178491935HCID 178491935—
SolventIsopropanolHCID 3776—
ProductHCID 178492150HCID 178492150—

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 1-[trans-4-(tert-butyl-dimethyl-silanyloxy)-cyclohexyl]-7-chloro-3-(2-fluoro-4-methoxy-phenyl)-3,4-dihydro-1H-pyrimido[4,5-d]pyrimidin-2-one (0.20 g, 0.38 mmol) (from Example 17c supra), p-anisidine (61.5 mg, 0.50 mmol) (Aldrich) and p-toluenesulfonic acid monohydrate (95.1 mg, 0.50 mmol) (Aldrich) in 2-propanol (4 mL) was placed in a microwave reactor (SmithSynthesizer™). The reaction mixture was heated at 160° C. for 15 minutes. After cooling, it was concentrated under reduced pressure and purified by RP-HPLC (C-18, eluted with acetonitrile-water) to give 3-(2-fluoro-4-methoxy-phenyl)-1-(trans-4-hydroxy-cyclohexyl)-7-(4-methoxy-phenylamino)-3,4-dihydro-1H-pyrimido[4,5-d]pyrimidin-2-one. (Yield 0.12 g, 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115740B2
Source datasetuspto-grants-2006_10
ORD IDord-c92c93dae74648138a6aa4ac0a343390
Source noteuspto-grants-2006_10