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Nantong MYBio-pharm. Co., Ltd.
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0513-85921823 18662920231 |
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sales@ntminyanmedical.com |
| Products Intro: |
Product Name:tert-Butyl(1-amino-2-methyl-1-oxopropan-2-yl)carbamate
CAS:73470-46-9
Purity:95 Package:1g
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| Company Name: |
Shanghai YuanYe Biotechnology Co., Ltd.
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13636370518 |
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shyysw007@163.com |
| Products Intro: |
Product Name:tert-Butyl (1-amino-2-methyl-1-oxopropan-2-yl)carbamate
CAS:73470-46-9
Purity:>=95% Package:100mg Remarks:Y91042
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| Company Name: |
BePharm Ltd
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400-685-9117 |
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market@bepharm.com |
| Products Intro: |
Product Name:tert-Butyl (1-amino-2-methyl-1-oxopropan-2-yl)carbamate
CAS:73470-46-9
Purity:98% Package:1793RMB/1g
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| Company Name: |
Amatek Scientific Co. Ltd.
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0512-56316828 |
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info@amateksci.com |
| Products Intro: |
Product Name:2-(Boc-amino)-2-methylpropanamide
CAS:73470-46-9
Purity:97% HPLC Package:1g;5g;25g;100g
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| | tert-Butyl (1-amino-2-methyl-1-oxopropan-2-yl)carbamate Basic information |
| Product Name: | tert-Butyl (1-amino-2-methyl-1-oxopropan-2-yl)carbamate | | Synonyms: | tert-Butyl (1-amino-2-methyl-1-oxopropan-2-yl)carbamate;Carbamic acid, (2-amino-1,1-dimethyl-2-oxoethyl)-, 1,1-dimethylethylester;Boc-Aib-NH2;(1-Carbamoyl-1-methyl-ethyl)-carbamic acid tert-butyl ester;2-(Boc-amino)-2-methylpropanamide;Carbamic acid, N-(2-amino-1,1-dimethyl-2-oxoethyl)-, 1,1-dimethylethyl ester | | CAS: | 73470-46-9 | | MF: | C9H18N2O3 | | MW: | 202.25 | | EINECS: | | | Product Categories: | | | Mol File: | 73470-46-9.mol |  |
| | tert-Butyl (1-amino-2-methyl-1-oxopropan-2-yl)carbamate Chemical Properties |
| Melting point | 170-171 °C | | Boiling point | 348.5±25.0 °C(Predicted) | | density | 1.062±0.06 g/cm3(Predicted) | | storage temp. | 2-8°C | | pka | 11.05±0.46(Predicted) |
| | tert-Butyl (1-amino-2-methyl-1-oxopropan-2-yl)carbamate Usage And Synthesis |
| Synthesis | 2-((tert-butoxycarbonyl)amino)-2-methylpropanoic acid (CAN: 30992-29-1, 20 g, 98 mmol) was used as a raw material and mixed with di-tert-butyl dicarbonate (CAN: 24424-99-5, 27.67 g, 147 mmol) in acetonitrile (500 mL) and pyridine (4.6 mL) was added as a catalyst. The reaction mixture was stirred at room temperature for 20 minutes. Subsequently, ammonia (10 mL) was slowly added dropwise over 20 minutes. After the dropwise addition, the reaction mixture was continued to be stirred for 4 hours. Upon completion of the reaction, most of the solvent was removed by distillation under reduced pressure. The precipitated solid was collected by filtration and washed with acetonitrile. Finally, the solid was dried under reduced pressure to afford the target product boc-2-aminoisobutyric acid amide (17.5 g, 88% yield) as a white solid. Mass spectrometry (EI) analysis showed: m/e 225.1 [M + Na]+. | | References | [1] Patent: US2012/316147, 2012, A1. Location in patent: Page/Page column 33-34
[2] Patent: WO2012/168350, 2012, A1. Location in patent: Page/Page column 80
[3] Tetrahedron, 2004, vol. 60, # 40, p. 8929 - 8936
[4] Tetrahedron Letters, 2000, vol. 41, # 50, p. 9809 - 9813
[5] Tetrahedron Letters, 2003, vol. 44, # 3, p. 463 - 466 |
| | tert-Butyl (1-amino-2-methyl-1-oxopropan-2-yl)carbamate Preparation Products And Raw materials |
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