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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592709Generated: October 30, 2026

Piperazine → 1-Boc-4-(2-piperazin-1-yl-benzoyl)-piperazine

https://huagongshe.com/reaction/1592709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantTert-butyl 4-(2-bromobenzoyl)piperazine-1-carboxylateHCID 17952334—
Product1-Boc-4-(2-piperazin-1-yl-benzoyl)-piperazineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291619B2
Source datasetuspto-grants-2007_11
ORD IDord-9082b4a557f14a0db95363dc56e97111
Source noteuspto-grants-2007_11