Basic information Safety Supplier Related

1-BOC-5-AMINO-2,3-DIHYDRO-INDOLE

Basic information Safety Supplier Related

1-BOC-5-AMINO-2,3-DIHYDRO-INDOLE Basic information

Product Name:
1-BOC-5-AMINO-2,3-DIHYDRO-INDOLE
Synonyms:
  • tert-Butyl 5-amino-2,3-dihydro-1H-indole-1-carboxylate
  • 1-Boc-5-aMinoindoline
  • 2-Methyl-2-Propanyl 5-Amino-1-Indolinecarboxylate
  • 5-Amino-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester >=97%
  • 6-Amino-3,4-dihydro-2H-quinoline-1-carboxylic acid tert-butyl ester
  • 1-Boc-2,3-dihydro-1H-indol-5-amine
  • 5-AMINO-1-BOC-2,3-DIHYDROINDOLE
  • 5-AMINO-2,3-DIHYDRO-INDOLE-1-CARBOXYLIC ACID TERT-BUTYL ESTER
CAS:
129487-92-9
MF:
C13H18N2O2
MW:
234.29
Product Categories:
  • pharmacetical
Mol File:
129487-92-9.mol
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1-BOC-5-AMINO-2,3-DIHYDRO-INDOLE Chemical Properties

Boiling point:
385.2±41.0 °C(Predicted)
Density 
1.177±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2–8 °C
pka
5.44±0.20(Predicted)
form 
liquid
color 
Brown
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Safety Information

HazardClass 
IRRITANT
HS Code 
2933998090
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1-BOC-5-AMINO-2,3-DIHYDRO-INDOLE Usage And Synthesis

Synthesis

166104-19-4

129487-92-9

The general procedure for the synthesis of tert-butyl 5-aminoindoline-1-carboxylate from tert-butyl 5-nitro-1H-indole-1-carboxylate is as follows: XII; tert-butyl 5-amino-2,3-dihydro-indole-1-carboxylate; 6.8 g of tert-butyl 5-nitro-1H-indole-1-carboxylate was dissolved in 120 mL of methanol. To this solution was added 600 mg of 10% palladium carbon catalyst, followed by a hydrogenation reaction at room temperature for 1.5 hours. Upon completion of the reaction, the catalyst was removed by filtration and the solvent was evaporated under reduced pressure. The final product was 6 g of tert-butyl 5-aminoindoline-1-carboxylate in 100% yield of the theoretical value. The product was analyzed by mass spectrometry (ESI+) and showed m/z = 235 [M + H]+.

References

[1] Patent: WO2008/113760, 2008, A2. Location in patent: Page/Page column 92
[2] Patent: US2017/50964, 2017, A1. Location in patent: Paragraph 0734
[3] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 23, p. 6481 - 6488
[4] Synthesis, 2007, # 10, p. 1509 - 1512

1-BOC-5-AMINO-2,3-DIHYDRO-INDOLESupplier

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