HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → Piperazine, 1-[(6-broMo-3-pyridinyl)Methyl]-4-ethyl-
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 | — |
Reaction Steps
Add neat 1-ethylpiperazine (221.44 mL) to a mixture of 6-bromo-pyridine-3-carbaldehyde (300 g) and DCM (5000 mL). Then, add sodium triacetoxyborohydride (372.09 g) in portions and stir at RT for 12 h. Add DCM (1000 mL) and aqueous solution of sodium hydroxide 2 N (1500 mL). Separate the layers and extract twice the aqueous layer with DCM (600 mL). Combine the organic layers and remove the solvent under vacuum, add EA and evaporate to afford 451.3 g of the title compound. MS (ES+): m/z=285 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07855211B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-6dbbec81435b4a2383206b4611f3a310 |
| Source note | uspto-grants-2010_12 |