HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Acetylpiperazine → Tert-butyl 3-[(4-acetylpiperazin-1-yl)methyl]-5-methylphenylcarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Acetylpiperazine | HCID 83795 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 22288418 | HCID 22288418 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | Tert-butyl 3-[(4-acetylpiperazin-1-yl)methyl]-5-methylphenylcarbamate | HCID 22288425 | — |
Reaction Steps
To a solution of tert-butyl 3-formyl-5-methylphenylcarbamate (200 mg, 0.85 mmol) and acetylpiperazine (131 mg, 1.02 mmol) in 0.1 mL HOAc and 4 mL dichloroethane was added NaBH(OAc)3 (216 mg, 1.02 mmol) at room temperature. After 2 hours additional acetylpiperazine (131 mg, 1.02 mmol) and NaBH(OAc)3 (216 mg, 1.02 mmol) were added. After 2 hours the mixture was diluted with saturated NaHCO3. The layers were separated and the aqueous extracted with CH2Cl2 (3×). The combined organic layers were dried (MgSO4), filtered, and concentrated. Flash column chromatography (5% MeOH/CH2Cl2) gave tert-butyl 3-[(4-acetylpiperazin-1-yl)methyl]-5-methylphenylcarbamate as a white foam:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06958340B2 |
| Source dataset | uspto-grants-2005_10 |
| ORD ID | ord-7ea9157a90f745ec8824265b942c1b79 |
| Source note | uspto-grants-2005_10 |