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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415114Generated: October 29, 2026

Water → HCID 178452335, compound

https://huagongshe.com/reaction/415114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTert-butyl 4-(2-(3,4-diaminophenoxy)ethyl)piperazine-1-carboxylateHCID 59349631—
ReactantHCID 178511328HCID 178511328—
SolventAcetic AcidHCID 176—
ProductHCID 178452335HCID 178452335103.6%

Reaction Steps

A 100 mL flasked was charged of tert-butyl 4-(2-(3,4-diaminophenoxy)ethyl)piperazine-1-carboxylate (1.53 g, 4.54 mmol), water (50 mL) and acetic acid (2 mL) and stirred at room temperature for 15 minutes. The reaction mixture was placed in an ice bath and then charged with cyanogen bromine (0.526 g, 5 mmol) and continued to stir at 0° C. The reaction temperature was allowed to warm to room temperature and it was stirred over night. The reaction was completed as determined by LCMS. The reaction mixture was concentrated under reduced pressure and the resulting residue was dissolved in acetone, dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure to give 1.7 g of tert-butyl 4-(2-(2-amino-1H-benzo[d]imidazol-5-yloxy)ethyl)piperazine-1-carboxylate as a di-acetate salt as black foam. MS (EI): 362 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088767B2
Source datasetuspto-grants-2012_01
ORD IDord-d0743eb5ae45404784a4f3cef54eb5f3
Source noteuspto-grants-2012_01