![1198-15-8](/CAS/20180629/GIF/1198-15-8.gif)
1-methyl-2,3-dihydroquinolin-4(1H)-one synthesis
- Product Name:1-methyl-2,3-dihydroquinolin-4(1H)-one
- CAS Number:1198-15-8
- Molecular formula:C10H11NO
- Molecular Weight:161.2
![2,3-Dihydro-1H-quinolin-4-one](/CAS/GIF/4295-36-7.gif)
4295-36-7
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$30.00/250mg
![Iodomethane](/CAS/GIF/74-88-4.gif)
74-88-4
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$15.00/10g
![1-methyl-2,3-dihydroquinolin-4(1H)-one](/CAS/20180629/GIF/1198-15-8.gif)
1198-15-8
19 suppliers
$120.00/100mg
Yield:1198-15-8 68%
Reaction Conditions:
with potassium carbonate in N,N-dimethyl-formamide at 80;
Steps:
42.1 Step 1
A mixture of compound 1 (2.0 g, 13.6 mmol), iodomethane (5.8 g. 40.8 mmoi), and K2C03 (5.5 g, 40.8 mmoi) in DMF (30 ml) was stirred at 80°C overnight. Tothe mixture was added EA (100 ml) and aqueous saturated NaC1 (100 ml), and the resulting reaction mixture was stilTed for 30 nun. The organic layer was separated, washed by aqueous saturated NaC1 (50 mi*2), dried and concentrated, purified by silica gel column to afford compound 2 (1.5 g, 68%) as a yellow solid.
References:
WO2016/94824,2016,A1 Location in patent:Page/Page column 80; 81
![N-(2-Cyanoethyl)-N-methylaniline](/CAS/GIF/94-34-8.gif)
94-34-8
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$5.00/5g
![1-methyl-2,3-dihydroquinolin-4(1H)-one](/CAS/20180629/GIF/1198-15-8.gif)
1198-15-8
19 suppliers
$120.00/100mg
![Benzenamine, N-3-buten-1-yl-2-iodo-](/CAS/20210305/GIF/118670-86-3.gif)
118670-86-3
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![1-methyl-2,3-dihydroquinolin-4(1H)-one](/CAS/20180629/GIF/1198-15-8.gif)
1198-15-8
19 suppliers
$120.00/100mg
![2-Iodoaniline](/CAS/20180808/GIF/615-43-0.gif)
615-43-0
419 suppliers
$5.00/5g
![1-methyl-2,3-dihydroquinolin-4(1H)-one](/CAS/20180629/GIF/1198-15-8.gif)
1198-15-8
19 suppliers
$120.00/100mg
![Benzenamine, N-3-buten-1-yl-2-iodo-N-methyl-](/CAS/20210305/GIF/57056-89-0.gif)
57056-89-0
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![1-methyl-2,3-dihydroquinolin-4(1H)-one](/CAS/20180629/GIF/1198-15-8.gif)
1198-15-8
19 suppliers
$120.00/100mg