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18162-48-6872-50-4Methylene ChloridenaphthaleneTHFTitanium Dioxide

2-Chloro-6-Methoxy-4-Methylquinolin-8-aMine synthesis

3synthesis methods
6-METHOXY-4-METHYL-QUINOLIN-8-YLAMINE

57514-21-3
7 suppliers
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2-Chloro-6-Methoxy-4-Methylquinolin-8-aMine

74509-63-0
5 suppliers
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Yield:-

Steps:

Multi-step reaction with 4 steps
1: 96 percent / xylene / Heating
2: 83 percent / m-chloroperbenzoic acid / CHCl3 / Ambient temperature
3: 78 percent / POCl3 / CHCl3 / Heating
4: 87 percent / N2H4*H2O / ethanol; H2O / Heating

References:

LaMontagne;Blumbergs;Smith [Journal of Medicinal Chemistry,1989,vol. 32,# 8,p. 1728 - 1732]

1H-Isoindole-1,3(2H)-dione, 2-(2-chloro-6-methoxy-4-methyl-8-quinolinyl)-

121963-12-0
0 suppliers
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2-Chloro-6-Methoxy-4-Methylquinolin-8-aMine

74509-63-0
5 suppliers
inquiry

References
1H-Isoindole-1,3(2H)-dione, 2-(6-methoxy-4-methyl-8-quinolinyl)-

74509-62-9
0 suppliers
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2-Chloro-6-Methoxy-4-Methylquinolin-8-aMine

74509-63-0
5 suppliers
inquiry

References