HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lithium Hexamethyldisilazide → HCID 57489620, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 2,6-Dichloropyridine-3-carboxamide | HCID 22142778 | — |
| Reactant | Benzyl 4-(4-aminophenyl)piperazine-1-carboxylate | HCID 57489619 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 57489620 | HCID 57489620 | 92.9% |
Reaction Conditions
| Temperature | -78 °C |
|---|
Reaction Steps
To a mixture of 2,6-dichloronicotinamide (3 g, 15.71 mmol) and benzyl 4-(4-aminophenyl)piperazine-1-carboxylate (5.38 g, 17.28 mmol) in THF (100 mL) was added lithium bis(trimethylsilyl)amide (55.0 mL, 55.0 mmol) at −78° C. The reaction mixture was stirred at −78° C. for 20 min. and at rt for 2 h. The reaction was quenched with water and extracted three times with ethyl acetate. The combined organic layers were washed with water and concentrated. The residue was purified by MPLC chromatography (ISCO, 6% NH4OH/MeOH/CH2Cl2, 40 g+12 g stacked column) to give 6.8 g of benzyl 4-(4-(3-carbamoyl-6-chloropyridin-2-ylamino)phenyl)piperazine-1-carboxylate as a brown solid. LCMS: (M+H)+=466.2, 468.2 (Cl pattern).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08586751B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-ed82fdfbc1834834a3fb5ece3f93fd51 |
| Source note | uspto-grants-2013_11 |