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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783689Generated: October 30, 2026

Piperidine → HCID 21106538, compound

https://huagongshe.com/reaction/1783689

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant2-(Di-tert-butylphosphino)biphenylHCID 2734215—
ReactantHCID 21106537HCID 21106537—
ReactantSodium t-butoxideHCID 23676156—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductHCID 21106538HCID 2110653813%

Reaction Steps

4-(2-tert-Butyl-5-methyl-2H-pyrazol-3-ylamino)-2-(4-chlorophenyl)-2H-phthalazin-1-one (0.10 g, 0.25 mmol), piperidine (0.025 g, 0.29 mmol), NaOtBu (0.033 g, 0.34 mmol), tris-(dibenzylideneacetone)-dipalladium (0.06 g, 0.008 mmol) and 2-(di-t-butylphosphino)-biphenyl (0.004 g, 0.014 mmol) under argon were heated to 100° C. for 19 hours, and then allowed to cool to RT. The solvent was evaporated in vacuum, the residue was diluted in H2O (30 ml) and the resulting solid was collected by filtration. Purification of the raw product by preparative HPLC gave the title compound (0.014 g, 13% yield). 1H-NMR: (400 MHz, D6-DMSO) 8.35 (1H, d), superimposed by 8.34 (1H, s), 8.29 (1H, d), 8.01 (1H, t), 7.92 (1H, t), 7.31 (2H, d), 6.92 (2H, d), 5.94 (1H, s), 3.16 (4H, m), 1.61 (4H, m), 1.55 (9H, s), superimposes 1.54 (2H, m); MS (ESI+)=457.16 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501410B2
Source datasetuspto-grants-2009_03
ORD IDord-7a1b197c94924105a72dc888b7eebf3f
Source noteuspto-grants-2009_03