HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 1-Boc-4-(2-piperazin-1-yl-benzoyl)-piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Tert-butyl 4-(2-bromobenzoyl)piperazine-1-carboxylate | HCID 17952334 | — |
| Product | 1-Boc-4-(2-piperazin-1-yl-benzoyl)-piperazine | HCID 69410176 | — |
Reaction Steps
Boc protected piperazine (849 mg, 4.56 mmol) was dissolved in DCM (20 mL) and triethyl amine (2.54 mL, 18.2 mmol) was added. To the stirred solution, ortho-bromo benzoyl chloride (2 g, 9.11 mmol) was added via syringe under nitrogen. The system was stirred for about 12 hours at r.t. The reaction was washed with water, dried, filtered, and concentrated. The residue was subjected to chromatography on silica gel to give 1-Boc-4-(2-bromo-)-piperazine (1.48 g, 8.85 mmol) as a white foam. 1-Boc-4-(2-bromo-benzoyl)-piperazine was coupled to piperazine in a manner similar to Preparation 1A. LRMS (ESI+): 375.2 (M+1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07291619B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-9082b4a557f14a0db95363dc56e97111 |
| Source note | uspto-grants-2007_11 |