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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783687Generated: October 30, 2026

Aniline → HCID 11661462, compound

https://huagongshe.com/reaction/1783687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
ReactantHCID 11617275HCID 11617275—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 11661462HCID 116614622%

Reaction Steps

2-(4-Chloro-phenyl)-4-(5-methyl-1H-pyrazol-3-ylamino)-2H-phthalazin-1-one (B-1, 0.10 g, 0.28 mmol), aniline (0.034 g, 0.37 mmol), NaOtBu (0.041 g, 0.43 mmol), tris-(dibenzylideneacetone)-dipalladium (0.026 g, 0.028 mmol) and 2-(di-t-butylphosphino)-biphenyl (0.017 g, 0.057 mmol) under argon were heated to 100° C. for 17 hours, and then allowed to cool to RT. The solvent was evaporated in vacuum, the residue was diluted in H2O (50 ml) and the resulting solid was collected by filtration. Purification of the raw product by chromatography over silica gel with DCM:MeOH (20:1) gave the title compound (0.002 g, 2% yield) as a white solid (example U-1). 1H-NMR: (400 MHz, D6-DMSO) 12.0 (1H, s), 9.23 (1H, s), 8.49 (1H, d), 8.33-8.37 (2H, m), 7.88-7.97 (2H, m), 7.54 (2H, d), 7.28 (2H, t), 7.15 (4H, m), 6.86 (1H, t), 6.25 (1H, s), 2.19 (3H, s); MS (API+)=409.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501410B2
Source datasetuspto-grants-2009_03
ORD IDord-9d7718a6e8fd4fbc9bbe76373cfb88cd
Source noteuspto-grants-2009_03