HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1914763Generated: November 2, 2026
1-Methylpiperazine → HCID 178480760, compound
https://huagongshe.com/reaction/1914763
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | 2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenyl | HCID 2734217 | — |
| Reactant | HCID 178418261 | HCID 178418261 | — |
| Reactant | HCID 178513841 | HCID 178513841 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178480760 | HCID 178480760 | 60% |
Reaction Steps
Tris(dibenzilideneacetone)dipalladium, Pd2(dba)3, (2.3 g, 2.5 mmol), 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)-biphenyl (950 mg, 2.4 mmol), 8-[5-bromo-2-trifluoromethoxy-phenylamino]-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxamide (14.8 g, 31.54 mmol) in THF (160 mL) were charged in a round-bottom flask flushed with argon. The flask was evacuated and backfilled with argon. LiN(TMS)2 solution (1M in THF, 630 mL) and N-methylpiperazine (69 mL, 50.64 mmol) were added and the reaction mixture refluxed for 1 h. The reaction mixture was then allowed to cool to room temperature and filtered through a pad of celite. The organic phase was concentrated. The crude solid was purified by flash chromatography on silica gel (eluant: DCM/MeOH 95/5) to afford 9.2 g (60% yield) of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08614220B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-1fc197d36e4f47ffbb5ffafaa0eb84ac |
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| Source note | uspto-grants-2013_12 |
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