Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 1-Acetylpiperazine | HCID 83795 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 18506796 | HCID 18506796 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | HCID 18506846 | HCID 18506846 | — |
Reaction Steps
To a suspension of tert-butyl 4-acetylpyridin-2-ylcarbamate (16-3, 187 mg, 0.79 mmole) in MeOH (3 mL) was added 1-acetylpiperazine (304 mg, 2.37 mmole), glacial HOAc (0.14 mL, 2.3.7 mmole), and NaBH3CN (149 mg, 2.37 mmole) then the mixture was heated to 50° C. After 6 hr additional NaBH3CN (149 mg, 2.37 mmole) was added and heating continued. After 18 hr the mixture was cooled to RT, diluted with saturated NaHCO3, and extracted with CH2Cl2 (3×). The combined organic layers were dried (MgSO4), filtered, and concentrated. Flash column chromatography (gradient, 0-10% EtOH/EtOAc) gave the titled compound as an oil: 1H-NMR (500 MHz, CDCl3) δ8.17 (d, 1H, J=5.13 Hz), 7.87 (s, 1H), 7.52 (bs, 1H), 6.97 (d, 1H, J=5.13 Hz), 3.64-3.57 (m, 2H), 3.45-3.39 (m, 3H), 2.49-2.35 (m, 4H), 2.06 (s, 3H) 1.54 (s, 9H), 1.35 (d, 3H, J=6.59 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06586423B2 |
|---|
| Source dataset | uspto-grants-2003_07 |
|---|
| ORD ID | ord-f550941803f1405983cbd022ab9da8e2 |
|---|
| Source note | uspto-grants-2003_07 |
|---|