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2-TERT-BUTYL-1,3-DIISOPROPYLISOUREA

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2-TERT-BUTYL-1,3-DIISOPROPYLISOUREA Basic information

Product Name:
2-TERT-BUTYL-1,3-DIISOPROPYLISOUREA
Synonyms:
  • 2-TERT-BUTYL-1,3-DIISOPROPYLISOUREA
  • CarbaMiMidic acid, N,N'-bis(1-Methylethyl)-, 1,1-diMethylethyl ester
  • tert-Butyl N,N'-diisopropylimidocarbamate
  • tert-butyl N,N'-bis(1-methylethyl)imidocarbamate
  • O-tert-Butyl-N,N'-diisopropylisourea >
  • 3-DIISOPROPYLISOUREA
  • 2-TERT-BUTYL-1
  • N,N'-bis(propan-2-yl)(tert-butoxy)methanimidamide
CAS:
71432-55-8
MF:
C11H24N2O
MW:
200.32
Mol File:
71432-55-8.mol
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2-TERT-BUTYL-1,3-DIISOPROPYLISOUREA Chemical Properties

Boiling point:
61°C/10mmHg(lit.)
Density 
0.89±0.1 g/cm3(Predicted)
refractive index 
1.4240-1.4280
storage temp. 
Keep in dark place,Inert atmosphere,2-8°C
pka
9.54±0.50(Predicted)
form 
clear liquid
color 
Colorless to Almost colorless
InChI
InChI=1S/C11H24N2O/c1-8(2)12-10(13-9(3)4)14-11(5,6)7/h8-9H,1-7H3,(H,12,13)
InChIKey
FESDUDPSRMWIDL-UHFFFAOYSA-N
SMILES
C(=NC(C)C)(OC(C)(C)C)NC(C)C
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Safety Information

HS Code 
2925290090
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2-TERT-BUTYL-1,3-DIISOPROPYLISOUREA Usage And Synthesis

Physical Form

liquid

Uses

2-tert-Butyl-1,3-diisopropylisourea is a useful synthetic intermediate in the synthesis of 5-Oxo Atorvastatin tert-Butyl Ester (O847160) which is a Boc-protected derivative of Atorvastatin. 2-tert-Butyl-1,3-diisopropylisourea is also used as a reagent in the total synthesis of Citrafungin A which is an antifungal natural product.

Synthesis

693-13-0

75-65-0

71432-55-8

GENERAL STEPS: CuCl (63.4 mg, 0.64 mmol, 1 mol%) was added to a solution of N,N'-diisopropylcarbodiimide (10.0 mL, 63.9 mmol, 1.0 equiv) in tert-butanol (6.97 mL, 73.5 mmol, 1.15 equiv). The reaction mixture was stirred at room temperature for 14 hours. After completion of the reaction, purification was carried out by distillation under reduced pressure (80°C, 25 mmHg). 2-tert-butyl-1,3-diisopropylisourea was obtained as a colorless oil (10.4 g, 51.9 mmol, 81% yield). The product was characterized by 1H NMR (300 MHz, CDCl3): δ 3.80-3.58 (1H, m, CH), 3.31-2.97 (1H, m, CH), 1.44 (9H, s, tBu), 1.19-1.01 (12H, m, Me2×2).

References

[1] Organic Letters, 2005, vol. 7, # 13, p. 2615 - 2618
[2] Chemistry - A European Journal, 2007, vol. 13, # 30, p. 8543 - 8563
[3] Beilstein Journal of Organic Chemistry, 2011, vol. 7, p. 1486 - 1493
[4] Journal of Medicinal Chemistry, 2015, vol. 58, # 10, p. 4204 - 4219
[5] Patent: EP2952517, 2015, A1. Location in patent: Paragraph 0217

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