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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 557730Generated: October 31, 2026

Ammonium Chloride → tert-Butyl 4-(4-amino-2-cyanophenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/557730

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-Butyl 4-(2-cyano-4-nitrophenyl)piperazine-1-carboxylateHCID 22227995—
CatalystZincHCID 23994—
SolventMethanolHCID 887—
Producttert-Butyl 4-(4-amino-2-cyanophenyl)piperazine-1-carboxylateHCID 22227872—

Reaction Steps

4-(2-Cyano-4-nitro-phenyl)-piperazine-1-carboxylic acid tert-butyl ester (587 mg, 1.77 mmol) was dissolved in methanol (50 mL) and to this solution was added ammonium chloride (945 mg, 17.66 mmol) and zinc (1155 mg, 17.66 mmol). The mixture was magnetically stirred for 3 hr and the mixture was filtered through a pad of celite. The solids were rinsed with methanol and the combined filtrate was concentrated to a yellow solid. This crude intermediate was dissolved in ethyl acetate (400 mL) and the resulting solution was washed with water (400 mL) and brine (200 mL). The organic layer was collected, dried over sodium sulfate, and concentrated to give 4-(4-amino-2-cyano-phenyl)-piperazine-1-carboxylic acid tert-butyl ester that was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08058299B2
Source datasetuspto-grants-2011_11
ORD IDord-018e9012089a48e9aeb9c131fdaca6d9
Source noteuspto-grants-2011_11