HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403208Generated: October 27, 2026
1-Methylpiperazine → 3-Methoxy-4-[(trimethylsilyl)ethynyl]phenyl-4-methylpiperazine
https://huagongshe.com/reaction/1403208
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | [(4-Bromo-2-methoxyphenyl)ethynyl](trimethyl)silane | HCID 71239496 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Catalyst | 2-Dicyclohexylphosphino-2-(N,N-Dimethylamino)Biphenyl | HCID 66545338 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Methoxy-4-[(trimethylsilyl)ethynyl]phenyl-4-methylpiperazine | HCID 86725292 | 68.4% |
Reaction Steps
A solution of [(4-bromo-2-methoxyphenyl)ethynyl](trimethyl)silane (1.426 g, 5.035 mmol) in dry THF (25 mL) was degassed and backfilled with argon for three times. Pd2(dba)3 (230.5 mg, 0.252 mmol) and 2-dicyclohexylphosphino-2-(N,N′-dimethylamino)biphenyl (79.3 mg, 0.201 mmol) were added under argon atmosphere and the mixture was degassed and backfilled with argon for three times. Then 1 M LiHMDS in THF (12.1 mL, 12.084 mmol) and N-methylpiperazine (1.34 mL, 1.21 g, 12.083 mmol) were added by a syringe and the mixture was degassed and backfilled with Argon for three times. The reaction mixture was heated to reflux for 1 h. After cooling to room temperature the reaction mixture was filtered on a pad of celite washing with THF (200 mL). The filtrate was evaporated under vacuum and the black oil so obtained was purified by chromatography on silica gel (DCM/MeOH 9/1) to afford the title compound as a brownish solid (1.042 g, 68.4%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08912200B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-2647c7aa74384512ad91b54f599d80a0 |
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| Source note | uspto-grants-2014_12 |
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