Basic information Safety Supplier Related

(R)-1-AMinopropan-2-ylcarbaMic Acid tert-Buty Ester

Basic information Safety Supplier Related

(R)-1-AMinopropan-2-ylcarbaMic Acid tert-Buty Ester Basic information

Product Name:
(R)-1-AMinopropan-2-ylcarbaMic Acid tert-Buty Ester
Synonyms:
  • Carbamic acid, [(1R)-2-amino-1-methylethyl]-, 1,1-dimethylethyl ester (9CI)
  • tert-butyl (R)-1-aMinopropan-2-ylcarbaMate
  • (R)-2-N-Boc-propane-1,2-diaMine
  • (R)-tert-butyl 1-aminopropan-2-ylcarbamate
  • R-2-N-BOC-propane-1,2-diamine-HCl
  • (R)-2-(Boc-aMino)-propanaMine HCl
  • tert-butyl N-[(2R)-1-aMinopropan-2-yl]carbaMate
  • tert-Butyl (R)-1-aMinopropan-2-ylcarbaMate HCl
CAS:
100927-10-4
MF:
C8H18N2O2
MW:
174.24
Product Categories:
  • N-BOC
Mol File:
100927-10-4.mol
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(R)-1-AMinopropan-2-ylcarbaMic Acid tert-Buty Ester Chemical Properties

Boiling point:
264℃
Density 
0.984
Flash point:
113℃
storage temp. 
2-8°C(protect from light)
pka
12.19±0.46(Predicted)
Appearance
White to off-white Solid
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Safety Information

HS Code 
2924190090
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(R)-1-AMinopropan-2-ylcarbaMic Acid tert-Buty Ester Usage And Synthesis

Uses

(R)-1-Aminopropan-2-ylcarbamic Acid tert-Buty Ester is used as an intermediate in the preparation of potent benzothiophene inhibitors of mitogen activated protein kinase-activated protein kinase 2 (MK 2).

Synthesis

146610-69-7

100927-10-4

To a stirred solution of tert-butyl (S)-1-azidopropan-2-ylcarbamate (S2-3) (6.0 g, 30 mmol) in ethyl acetate (50.0 mL) was added 10% Pd/C (2.3 g). The reaction mixture was stirred at room temperature under hydrogen atmosphere (1 atm) for 15 hours. Upon completion of the reaction, the mixture was filtered through a diatomaceous earth pad and the diatomaceous earth was washed with ethyl acetate. The filtrate was concentrated under reduced pressure to afford tert-butyl N-[(1R)-2-amino-1-methylethyl]carbamate (S2-4) (4.8 g, 92% yield) as a light yellow solid.1H NMR (400 MHz, DMSO-d6) δ 0.95 (d, J = 6.6 Hz, 3H), 1.36 (s, 9H), 2.49 (m, 2H), 3.32 (m, 1H), 6.49 (br s, 1H).

References

[1] Patent: US2016/75720, 2016, A1. Location in patent: Paragraph 0247

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