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18162-48-6872-50-4Methylene ChloridenaphthaleneTHFTitanium Dioxide
1232149-36-8

7-bromo-3-nitroquinolin-4-amine synthesis

7synthesis methods
723280-98-6 Synthesis
7-bromo-4-chloro-3-nitroquinoline

723280-98-6
62 suppliers
$43.00/100mg

7-bromo-3-nitroquinolin-4-amine

1232149-36-8
16 suppliers
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Yield:1232149-36-8 99%

Reaction Conditions:

with ammonium hydroxide in acetonitrile at 40; for 3 h;Sealed tube;

References:

WO2021/142203,2021,A1 Location in patent:Page/Page column 52-54

179943-57-8 Synthesis
7-BROMO-4-OXO-1,4-DIHYDRO-QUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER

179943-57-8
86 suppliers
$33.00/1g

7-bromo-3-nitroquinolin-4-amine

1232149-36-8
16 suppliers
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References
956268-33-0 Synthesis
7-broMoquinolin-4(1H)-one

956268-33-0
24 suppliers
$41.00/250mg

7-bromo-3-nitroquinolin-4-amine

1232149-36-8
16 suppliers
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References
3-Bromoaniline

591-19-5
331 suppliers
$10.00/10g

7-bromo-3-nitroquinolin-4-amine

1232149-36-8
16 suppliers
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References
2-[[(3-Bromophenyl)amino]methylene]propanedioic Acid 1,3-Diethyl Ester

351893-47-5
10 suppliers
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7-bromo-3-nitroquinolin-4-amine

1232149-36-8
16 suppliers
inquiry

References