Name | 6-methoxy-8-quinolylamine |
Synonyms | amichin wr15081 IFLAB-BB F1901-0147 6-methoxy-8-quinolinamin 6-methoxy-8-quinolylamine 6-methoxy-8-quinolinamine 6-methoxyquinolin-8-amine 8-amino-6-methoxyquinoline 6-Methoxy-8-aminoquinoline 6-methoxy-8-aminoquinoline 8-amino-6-methoxy-quinolin 6-Methoxy-8-amino-quinoline 6-Methoxy-8-amino quinoline 6-Methoxyquinolin-8-ylamine |
CAS | 90-52-8 |
EINECS | 202-001-3 |
InChI | InChI=1/C10H10N2O/c1-13-8-5-7-3-2-4-12-10(7)9(11)6-8/h2-6H,11H2,1H3 |
Molecular Formula | C10H10N2O |
Molar Mass | 174.2 |
Density | 1.217±0.06 g/cm3(Predicted) |
Melting Point | 41 °C |
Boling Point | 137-138 °C(Press: 1 Torr) |
Solubility | DMSO (Slightly), Methanol (Slightly) |
Appearance | Solid |
Color | Brown to Very Dark Brown Low Melting |
pKa | 3.49±0.10(Predicted) |
Storage Condition | under inert gas (nitrogen or Argon) at 2–8 °C |
Stability | Incompatible with strong oxidizing agents. |
Physical and Chemical Properties | White crystal. Melting point 41 ℃, boiling point 137-138 ℃(133Pa). |
Hazard Class | IRRITANT |
crystal. Melting Point 51 °c. Boiling Point (0.133kPa) 137~138 deg C.
6 methoxy 8 nitroquinoline in hydrochloric acid medium with iron powder reduced to 6-methoxy -8-amino quinine hydrochloride, and then neutralized with liquid alkali to get crude product, crude product after filtration, salting out, dehydrated to obtain finished product.
pharmaceutical intermediates, mainly used for the preparation of antimalarial drugs primary ammonia quinoline phosphate, malaria quinoline.
Use | intermediates of antimalarial drugs primaquine phosphate, pentaquine, and vivaquine. |
production method | 6-methoxy-8-nitroquinoline is obtained by reduction with iron powder in hydrochloric acid medium and neutralization with liquid alkali. Hydrochloric acid was put into a glass-lined reaction pan, and the temperature was raised to 50 ° C., and 6-methoxy-8-nitroquinoline and iron powder were added. The whole was added at 65-70 ° C. In 3.5H, incubated for 2H, cooled and filtered to give crude 8-amino-6-methoxyquinoline hydrochloride. After salting-out purification, 8-amino -6-methoxyquinoline was precipitated by neutralization to pH 7 with dilute alkali, and the crude product was obtained by filtration and purified with toluene to obtain 8-amino-6-methoxyquinoline. The yield was 65%. Product specifications: content ≥ 65%. Raw material consumption quota: 6-methoxy-8-nitroquinoline (94%)1765kg/t, hydrochloric acid (37%)10479kg/t, iron filings (industrial) 2519kg/t. |