1-BOC-4-(4-BROMO-2-CYANOPHENYL)PIPERAZINE
- Product Name
- 1-BOC-4-(4-BROMO-2-CYANOPHENYL)PIPERAZINE
- CAS No.
- 791846-40-7
- Chemical Name
- 1-BOC-4-(4-BROMO-2-CYANOPHENYL)PIPERAZINE
- Synonyms
- tert-Butyl 4-(4-bromo-2-cyanophenyl);1-BOC-4-(4-BROMO-2-CYANOPHENYL)PIPERAZINE;TERT-BUTYL 4-(4-BROMO-2-CYANOPHENYL)PIPERAZINE-1-CARBOXYLATE;4-(4-Bromo-2-cyano-phenyl)-piperazine-1-carboxylic acid tert-butyl ester;1-Piperazinecarboxylic acid, 4-(4-bromo-2-cyanophenyl)-, 1,1-dimethylethyl ester
- CBNumber
- CB52453764
- Molecular Formula
- C16H20BrN3O2
- Formula Weight
- 366.25
- MOL File
- 791846-40-7.mol
1-BOC-4-(4-BROMO-2-CYANOPHENYL)PIPERAZINE Property
- storage temp.
- Sealed in dry,Room Temperature
N-Bromosuccinimide Price
- Product number
- FB144043
- Product name
- tert-Butyl 4-(4-bromo-2-cyanophenyl)piperazine-1-carboxylate
- Packaging
- 250mg
- Price
- $62.5
- Updated
- 2021/12/16
- Product number
- FB144043
- Product name
- tert-Butyl 4-(4-bromo-2-cyanophenyl)piperazine-1-carboxylate
- Packaging
- 500mg
- Price
- $110
- Updated
- 2021/12/16
- Product number
- W8485
- Product name
- 1-Boc-4-(4-Bromo-2-cyanophenyl)piperazine
- Packaging
- 250mg
- Price
- $111
- Updated
- 2021/12/16
- Product number
- FB144043
- Product name
- tert-Butyl 4-(4-bromo-2-cyanophenyl)piperazine-1-carboxylate
- Packaging
- 1g
- Price
- $189
- Updated
- 2021/12/16
- Product number
- 072475
- Product name
- 1-Boc-4-(4-Bromo-2-cyanophenyl)piperazine
- Purity
- 95+%
- Packaging
- 250mg
- Price
- $231
- Updated
- 2021/12/16
1-BOC-4-(4-BROMO-2-CYANOPHENYL)PIPERAZINE Chemical Properties,Usage,Production
Synthesis
179897-89-3
57260-71-6
791846-40-7
General procedure for the synthesis of 1-BOC-4-(4-bromo-2-cyanophenyl)piperazine from 2-fluoro-5-bromobenzonitrile and N-BOC-piperazine: in a pressure tube, 5-bromo-2-fluorobenzonitrile (2,500 mg, 12.5 mmol), tert-butyl piperazine-1-carboxylate (2,444.45 mg, 13.12 mmol) and triethylamine (5.23 mL. 37.5 mmol) were dissolved in dimethyl sulfoxide (10 mL) and the reaction was refluxed at 100 °C. After completion of the reaction, the mixture was cooled and separated by extraction with ethyl acetate and saturated aqueous sodium bicarbonate. The organic phase was dried with anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was purified by fast column chromatography on silica gel, eluting with a 5-60% ethyl acetate/hexane gradient to afford the light brown oily product tert-butyl 4-(4-bromo-2-cyanophenyl)piperazine-1-carboxylate (3660 mg, 80% yield).
References
[1] Patent: KR2016/37198, 2016, A. Location in patent: Paragraph 2392-2394
[2] Bioorganic and Medicinal Chemistry Letters, 2004, vol. 14, # 20, p. 5095 - 5098
[3] Patent: WO2017/38909, 2017, A1. Location in patent: Paragraph 0290; 0291
[4] Patent: WO2009/79593, 2009, A1. Location in patent: Page/Page column 120
1-BOC-4-(4-BROMO-2-CYANOPHENYL)PIPERAZINE Preparation Products And Raw materials
Raw materials
Preparation Products
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