HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264370Generated: October 31, 2026
Sodium Hydroxide → Piperazine, 1-[(6-broMo-3-pyridinyl)Methyl]-4-ethyl-
https://huagongshe.com/reaction/2264370
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Ethylpiperazine | HCID 79196 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 6-Bromo-3-pyridinecarboxaldehyde | HCID 11769234 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Piperazine, 1-[(6-broMo-3-pyridinyl)Methyl]-4-ethyl- | HCID 86642886 | 90.7% |
Reaction Steps
Add neat 1-ethylpiperazine (5.6 kg) to a mixture of 6-bromo-pyridine-3-carbaldehyde (8.3 kg) and DCM (186 kg). Then, add sodium triacetoxyborohydride (10.9 kg) in portions and stir at 20-30° C. for 12 h. Quench the reaction into a mixture of DCM (36 kg) and aqueous solution of sodium hydroxide 2 N (46 kg). Separate the layers and extract twice the aqueous layer with DCM (24×2 kg). Combine the organic layers, wash with brine (50×2 kg) and remove the solvent under vacuum to afford 11.5 kg of the title compound. MS (ES+): m/z=285 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07855211B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-25978f257a02499fbe085de19abb3c91 |
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| Source note | uspto-grants-2010_12 |
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