Basic information Safety Supplier Related

1-Boc-5-aminoindole

Basic information Safety Supplier Related

1-Boc-5-aminoindole Basic information

Product Name:
1-Boc-5-aminoindole
Synonyms:
  • 5-AMINO-1-BOC-BENZIMIDAZOLE
  • 5-AMINO-1-BOC-BENZOIMIDAZOLE
  • 5-AMINO-BENZOIMIDAZOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
  • 5-AMINO-INDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
  • 1-BOC-5-AMINOINDOLE
  • 5-AMINOINDOLE-1-BOC
  • N-Boc-5-Aminoindole
  • tert-butyl 5-amino-1H-indole-1-carboxylate
CAS:
166104-20-7
MF:
C13H16N2O2
MW:
232.28
Product Categories:
  • pharmacetical
Mol File:
166104-20-7.mol
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1-Boc-5-aminoindole Chemical Properties

Boiling point:
384.2±34.0 °C(Predicted)
Density 
1.16±0.1 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
4.28±0.10(Predicted)
form 
low melting solid
color 
Brown
CAS DataBase Reference
166104-20-7(CAS DataBase Reference)
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Safety Information

HS Code 
2933998090
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1-Boc-5-aminoindole Usage And Synthesis

Synthesis

166104-19-4

166104-20-7

General procedure for the synthesis of N-Boc-5-aminoindole from tert-butyl 5-nitro-1H-indole-1-carboxylate: tert-butyl 5-nitro-1H-indole-1-carboxylate (525 mg, 2.0 mmol) was dissolved in ethyl acetate (8 mL), and 10% palladium-carbon-catalyst (50 mg) was added. The reaction mixture was stirred overnight at room temperature in a hydrogen atmosphere. Upon completion of the reaction, the catalyst was removed by suction filtration and the filtrate was concentrated under reduced pressure to afford the white solid product N-Boc-5-aminoindole (469 mg, 100% yield).

References

[1] Patent: CN104311541, 2017, B. Location in patent: Paragraph 0164; 0165
[2] Patent: US2009/247568, 2009, A1. Location in patent: Page/Page column 36
[3] Journal of Medicinal Chemistry, 2013, vol. 56, # 15, p. 6273 - 6277
[4] Synthetic Communications, 2006, vol. 36, # 14, p. 2069 - 2077
[5] Journal of Medicinal Chemistry, 2011, vol. 54, # 4, p. 1106 - 1110

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