HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852947Generated: October 30, 2026
1-Methylpiperazine → HCID 67457051, compound
https://huagongshe.com/reaction/1852947
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 86685293 | HCID 86685293 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67457051 | HCID 67457051 | 63.2% |
Reaction Steps
To a solution of 2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)ethyl methanesulfonate (0.080 g, 0.253 mmol) in 0.5 mL N,N-dimethylformamide was added 1-methylpiperazine (0.281 mL, 2.53 mmol) and the reaction was sealed under nitrogen and heated to 50° C. for 2.5 hours. The reaction mixture was diluted with dichloromethane (3 mL) and then loaded directly onto a silica gel column pre-wetted and eluted with 15% methanol in dichloromethane containing 1% ammonium hydroxide to afford 1-(2-(4-methylpiperazin-1-yl)ethyl)-1H-pyrazol-4-ylboronic acid (0.038 g, 0.160 mmol, 63% yield) as a result of hydrolysis on silica in the presence of methanol and ammonium hydroxide. MS (apci) m/z=239.1 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962596B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-5cf00ddb536e42808a82bff6130fbc1c |
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| Source note | uspto-grants-2015_02 |
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