HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1406018Generated: October 31, 2026
1-Methylpiperazine → HCID 60152865, compound
https://huagongshe.com/reaction/1406018
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 68358132 | HCID 68358132 | — |
| Reactant | HCID 178418261 | HCID 178418261 | — |
| Catalyst | 2-(Dicyclohexylphosphino)-2'-(dimethylamino)biphenyl | HCID 2734217 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 60152865 | HCID 60152865 | 100.8% |
Reaction Steps
Pd2(dba)3, (0.002 g, 0.002 mmol), 2-dicyclohexylphosphino-2′-(N,N-dimethylamino)-biphenyl (0.002 g, 0.005 mmol), 9-[(4-bromo-2-methoxyphenyl)amino]-N-(2-ethylphenyl)-1-methyl-1,4,5,6-tetrahydropyrazolo[4′,3′:6,7]cyclohepta[1,2-d]pyrimidine-3-carboxamide (0.040 g, 0.07 mmol) in THF (1 mL) were charged in a round-bottomed flask flushed with argon. The flask was evacuated and backfilled with argon. LiN(TMS)2 solution (1M in THF, 0.9 mL) and N-methylpiperazine (0.030 mL, 0.30 mmol) were added and the reaction mixture was heated at 85° C. for 0.5 h. The reaction mixture was then allowed to cool to room temperature and concentrated. The crude solid was purified by flash chromatography on silica gel (eluant: DCM/MeOH 95/5) to afford 0.040 g (95% yield) of the title compound as yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916577B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-9d3cc0d6e9a54891802fa7accd9f59bd |
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| Source note | uspto-grants-2014_12 |
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