3-AMINO-2-METHYLQUINOLINE
3-AMINO-2-METHYLQUINOLINE Basic information
- Product Name:
- 3-AMINO-2-METHYLQUINOLINE
- Synonyms:
-
- 3-AMINO-2-METHYLQUINOLINE
- 3-Quinolinamine,2-methyl-(9CI)
- 2-Methylquinolin-3-amine
- 3-Amino-2-methylquinolinedihydrochloride
- 3-Quinolinamine, 2-methyl-
- 3-AMINO-2-METHYLQUINOLINE ISO 9001:2015 REACH
- CAS:
- 21352-22-7
- MF:
- C10H10N2
- MW:
- 158.2
- Product Categories:
-
- ISOQUINOLINE
- Mol File:
- 21352-22-7.mol
3-AMINO-2-METHYLQUINOLINE Chemical Properties
- Melting point:
- 160-161℃
- Boiling point:
- 333.29°C (estimate)
- Density
- 1.1606 (estimate)
- refractive index
- 1.7080 (estimate)
- storage temp.
- Keep in dark place,Inert atmosphere,Room temperature
- pka
- 5.81±0.50(Predicted)
- Appearance
- White to yellow Solid
3-AMINO-2-METHYLQUINOLINE Usage And Synthesis
Synthesis

75353-77-4

21352-22-7
2-Methyl-3-nitroquinoline (400 mg, 2.13 mmol) was used as starting material, which was dissolved in concentrated hydrochloric acid (8 mL) and heated to 50 °C. Subsequently, tin(II) chloride dihydrate (1.2 g, 5.3 mmol) was slowly added to the reaction system. The reaction temperature was maintained at 50 °C and the reaction mixture was continuously stirred overnight. After completion of the reaction, the mixture was diluted with distilled water (20 mL). The pH was adjusted to 9 with 5 N NaOH aqueous solution.The reaction mixture was cooled to 4 °C and extracted with ethyl acetate (2 × 30 mL). The organic phases were combined, washed with ice water (40 mL), dried over anhydrous Na2SO4, filtered and concentrated to give 3-amino-2-methylquinoline (270 mg, 80% yield) as a yellow solid. The product was characterized by 1H NMR (400 MHz, CDCl3): δ 7.84 (d, J = 8.4 Hz, 1H), 7.51 (dd, J = 1.2, 8.0 Hz, 1H), 7.39-7.30 (m, 2H), 7.16 (s, 1H), 3.77 (s, 2H), 2.56 (s, 3H).
References
[1] Patent: WO2013/14569, 2013, A1. Location in patent: Page/Page column 35
[2] Justus Liebigs Annalen der Chemie, 1957, vol. 602, p. 14,18
[3] Chemistry - A European Journal, 2014, vol. 20, # 24, p. 7245 - 7248
[4] Chemical Communications, 2014, vol. 50, # 67, p. 9588 - 9590
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