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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051907Generated: November 2, 2026

tert-Butyl piperazine-1-carboxylate → HCID 90239675, compound

https://huagongshe.com/reaction/1051907

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantHCID 75593293HCID 75593293—
SolventEthanolHCID 702—
ProductHCID 90239675HCID 9023967567.9%

Reaction Conditions

Temperature120 °C

Reaction Steps

2,5,6-tribromo-4-nitro-1H-1,3-benzodiazole (Method 2A) (17.5 mmol, 7 g) was dissolved in EtOH (30 ml) with N-Boc-piperazine (52.5 mmol, 9.78 g). The resulting mixture was stirred at 120° C. until the reaction was complete (8 h) by LC/MS. The mixture was allowed to cool to RT and concentrated in-vacuo. The product was purified on silica gel using DCM/MeOH (99:1) to afford tert-butyl 4-(5,6-dibromo-4-nitro-1H-1,3-benzodiazol-2-yl)piperazine-1-carboxylate (6 g). m/z 405.8; rt 2.4 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388192B2
Source datasetuspto-grants-2016_07
ORD IDord-125b6f77aaa74f05816aeda43fc9f83e
Source noteuspto-grants-2016_07