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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | tert-Butyl 4-(2-cyano-4-nitrophenyl)piperazine-1-carboxylate | HCID 22227995 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | tert-Butyl 4-(4-amino-2-cyanophenyl)piperazine-1-carboxylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08058299B2 |
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| Source dataset | uspto-grants-2011_11 |
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| ORD ID | ord-018e9012089a48e9aeb9c131fdaca6d9 |
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| Source note | uspto-grants-2011_11 |
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