HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 53854495, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Piperazinecarboxaldehyde | HCID 82191 | — |
| Reactant | HCID 20096921 | HCID 20096921 | — |
| Product | HCID 53854495 | HCID 53854495 | — |
Reaction Steps
A mixture of N-formylpiperazine (0.41 mL, 4.0 mmol), (4-nitro-2,6-dichlorophenyl)-2-bromoacetamide (1.31 g, 4.0 mmol), and K2CO3 (2.2 g) in 20 mL of DMF was stirred at room temperature for 15 minutes. The mixture was then partitioned between ethyl acetate and water, the aqueous extracts were diluted with brine, and then exhaustively extracted with ethyl acetate. Solvent was removed in vacuo from the combined ethyl acetate extracts to yield the III product as a residue (1.79 g): 1H NMR (300 MHz, CDCl3) δ 2.73-2.78 (m, 2H), 2.85-2.97 (m, 4H), 3.34 (s, 2H), 3.51-3.56 (m, 1H), 3.68-3.72 (m, 1H), 8.30 (s, 2H), 9.14 (broad s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05382584 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-9d0eac06d21b4be88bae0ea767b5b7d0 |
| Source note | uspto-grants-1995_01 |