Basic information Safety Supplier Related

6-chloroquinolin-8-amine

Basic information Safety Supplier Related

6-chloroquinolin-8-amine Basic information

Product Name:
6-chloroquinolin-8-amine
Synonyms:
  • 6-chloroquinolin-8-amine
  • 6-Chloro-8-quinolinamine
  • 6-Chloro-8-aminoquinoline
  • 8-Amino-6-chloroquinoline
  • 8-Quinolinamine, 6-chloro-
  • Nsc 27981
  • NSC 2798
  • 6-Chloroquinolin-8-amine 97%
CAS:
5470-75-7
MF:
C9H7ClN2
MW:
178.62
Product Categories:
  • Aromatics
  • Heterocycles
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
Mol File:
5470-75-7.mol
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6-chloroquinolin-8-amine Chemical Properties

storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
Appearance
Off-white to light yellow Solid
EPA Substance Registry System
8-Quinolinamine, 6-chloro- (5470-75-7)
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Safety Information

HS Code 
2933499090
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6-chloroquinolin-8-amine Usage And Synthesis

Uses

6-Chloro-8-aminoquinoline is a di-substituted quinoline derivative used in the preparation fungitoxic analogs.

Uses

6-chloroquinolin-8-amine is a di-substituted quinoline derivative used in the preparation fungitoxic analogs.

Synthesis

68527-66-2

5470-75-7

Synthesis Method 2: Preparation of 6-chloro-8-aminoquinoline (precursor to Example Compound 4); To a stirred suspension of 6-chloro-8-nitroquinoline (Synthesis Method 1; 1.00 g, 4.79 mmol) in water (20 mL) was added acetic acid (0.82 mL, 14.3 mmol) and iron powder (1.61 g, 28.8 mmol) sequentially. The reaction mixture was heated to near reflux temperature, maintained for 1.5 h and then cooled to room temperature. Solid sodium hydroxide (0.65 g, 16.3 mmol) and ethyl acetate (30 mL) were added to the reaction system under continuous stirring. Diatomaceous earth (30 mL) was then added and the slurry was separated by filtration. The filter cake was washed with ethyl acetate. The combined filtrates were sequentially washed with aqueous sodium bicarbonate, dried over sodium sulfate and concentrated. The resulting brown viscous oil was purified by rapid chromatography on silica gel (eluent: hexane/ethyl acetate) to give 0.57 g of yellow solid product (67% yield). Product characterization data: 1H NMR (CDCl3) δ 8.71 (dd, J = 4.2, 1.5 Hz, 1H), 7.94 (dd, J = 8.3, 1.5 Hz, 1H), 7.36 (dd, J = 8.3, 4.2 Hz, 1H), 7.09 (d, J = 2.1 Hz, 1H), 6.84 (d, J = 2.1 Hz, 1H), 5.09 (br s, 2.1 Hz, 1H), 5.09 (br s, 2.1 Hz, 1H). 5.09 (br s, 2H) ppm.

References

[1] Monatshefte fuer Chemie, 1994, vol. 125, # 6/7, p. 723 - 730
[2] Monatshefte fuer Chemie, 1994, vol. 125, # 6/7, p. 723 - 730
[3] Patent: US2007/254894, 2007, A1. Location in patent: Page/Page column 21
[4] Patent: US2003/32645, 2003, A1
[5] Journal of the American Chemical Society, 1946, vol. 68, p. 1577

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