1-TERT-BUTYLOXYCARBONYL-4-AMINO-PIPERAZINE

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Products Intro: Product Name:1-TERT-BUTYLOXYCARBONYL-4-AMINO-PIPERAZINE
CAS:118753-66-5
Purity:0.98 Package:1KG;10KG;50KG
Company Name: Changzhou Carman Chemical Co., Ltd.
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Products Intro: Product Name:tert-butyl 4-aminopiperazine-1-carboxylate
CAS:118753-66-5
Purity:95% Package:5KG;1KG
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Products Intro: Product Name:1-TERT-BUTYLOXYCARBONYL-4-AMINO-PIPERAZINE
CAS:118753-66-5
Purity:98%min Package:1g;0.5USD
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Products Intro: Product Name:tert-butyl 4-aminopiperazine-1-carboxylate
CAS:118753-66-5
Purity:0.97 Package:1KG;25KG
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Products Intro: Product Name:tert-Butyl 4-aMinopiperazin-1-carboxylate
CAS:118753-66-5
Purity:0.99 Package:5KG;1KG

1-TERT-BUTYLOXYCARBONYL-4-AMINO-PIPERAZINE manufacturers

1-TERT-BUTYLOXYCARBONYL-4-AMINO-PIPERAZINE Basic information
Product Name:1-TERT-BUTYLOXYCARBONYL-4-AMINO-PIPERAZINE
Synonyms:1-Piperazinecarboxylicacid,4-amino-,1,1-dimethylethylester(9CI);1-PIPERAZINECARBOXYLIC ACID,4-AMINO-,1,1-DIMETHYLETHYL ESTER;1-T-BUTYLOXYCARBONYL-4-AMINO-PIPERAZINE;tert-Butyl 4-aMinopiperazin-1-carboxylate;4-AMino-piperazine-1-carboxylic acid tert-butyl ester;1-Amino-4-(tert-butoxycarbonyl)piperazine;4-Amino-1-piperazinecarboxylic acid 1,1-dimethylethyl ester;1-TERT-BUTYLOXYCARBONYL-4-AMINO-PIPERAZINE
CAS:118753-66-5
MF:C9H19N3O2
MW:201.27
EINECS:
Product Categories:AMINOACID
Mol File:118753-66-5.mol
1-TERT-BUTYLOXYCARBONYL-4-AMINO-PIPERAZINE Structure
1-TERT-BUTYLOXYCARBONYL-4-AMINO-PIPERAZINE Chemical Properties
Boiling point 281℃
density 1.097
Fp 124℃
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka7.03±0.20(Predicted)
AppearanceWhite to off-white Solid
InChIInChI=1S/C9H19N3O2/c1-9(2,3)14-8(13)11-4-6-12(10)7-5-11/h4-7,10H2,1-3H3
InChIKeyQMZFIRHRGPLKEV-UHFFFAOYSA-N
SMILESN1(C(OC(C)(C)C)=O)CCN(N)CC1
Safety Information
RIDADR UN2735
MSDS Information
1-TERT-BUTYLOXYCARBONYL-4-AMINO-PIPERAZINE Usage And Synthesis
Synthesis
tert-butyl 4-nitrosopiperazine-1-carboxylate

877177-42-9

1-TERT-BUTYLOXYCARBONYL-4-AMINO-PIPERAZINE

118753-66-5

General procedure for the synthesis of tert-butyl 4-aminopiperazine-1-carboxylate from tert-butyl 4-nitroso piperazine-1-carboxylate: At room temperature, the compound (730 mg) obtained in step (1) was dissolved in methanol (10 mL) and zinc powder (1.1 g) was added. Acetic acid (10 mL) was added slowly and dropwise under cooling in an ice bath. The reaction mixture was stirred at room temperature for 2 hours. Upon completion of the reaction, the mixture was filtered and the filtrate was alkalized by adding aqueous sodium bicarbonate to the filtrate. After alkalinization, the mixture was extracted with chloroform. The organic layers were combined, dried with anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to give tert-butyl 4-aminopiperazine-1-carboxylate (730 mg, yield: 100%) as a light yellow oil.

References[1] Patent: WO2007/46550, 2007, A1. Location in patent: Page/Page column 120
[2] Patent: WO2006/20561, 2006, A2. Location in patent: Page/Page column 61
[3] European Journal of Medicinal Chemistry, 2018, vol. 158, p. 247 - 258
1-TERT-BUTYLOXYCARBONYL-4-AMINO-PIPERAZINE Preparation Products And Raw materials
Raw materialstert-butyl 4-nitrosopiperazine-1-carboxylate-->Sodium bicarbonate-->Acetic acid-->ZINC
Tag:1-TERT-BUTYLOXYCARBONYL-4-AMINO-PIPERAZINE(118753-66-5) Related Product Information
4-Hydroxy-4-(2-propenyl)piperidine-1-carboxylic acid tert-butyl ester tert-butyl 4-amidinopiperidine-1-carboxylate 1-TERT-BUTYLOXYCARBONYL-4-AMINO-PIPERAZINE