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inquiryformaldehyd
2-(5-methoxy-2-methyl-1H-indol-3-yl)ethan-1-amine hydrochloride
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
Conditions | Yield |
---|---|
With sodium methylate; sodium cyanoborohydride; acetic acid In methanol; water | 80% |
N,N-dimethyl-4-oxopentanamine hydrochloride
4-methoxyphenylhydrazine hydrochloride
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
Conditions | Yield |
---|---|
Stage #1: N,N-dimethyl-4-oxopentanamine hydrochloride; 4-methoxyphenylhydrazine hydrochloride With sulfuric acid; acetic acid at 40 - 60℃; for 3.5 - 4.5h; Heating / reflux; Stage #2: With sodium carbonate In water pH=10; | 78.2% |
(5-methoxy-2-methyl-indol-3-yl)-acetic acid dimethylamide
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride; diethyl ether |
2-(5-Methoxy-2-methyl-1H-indol-3-yl)-N,N-dimethyl-2-oxo-acetamide
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
Conditions | Yield |
---|---|
With lithium aluminium tetrahydride |
5-methoxy-2-methyl-1H-indole
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: diethyl ether 2: H2O; CHCl3 3: LiAlH4 View Scheme |
2-(5-methoxy-2-methyl-1H-indol-3-yl)-2-oxoacetyl chloride
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: H2O; CHCl3 2: LiAlH4 View Scheme |
5-Methoxy-2-methylindole-3-acetic acid
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
Conditions | Yield |
---|---|
Multi-step reaction with 2 steps 1: 195 °C 2: LiAlH4; diethyl ether View Scheme |
2-(5-methoxy-2-methyl-1H-indol-3-yl)ethan-1-amine hydrochloride
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
Conditions | Yield |
---|---|
With sodium hydroxide; formaldehyd; sodium methylate; sodium cyanoborohydride; acetic acid In methanol | 1.215 g (80%) |
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
methyl iodide
Conditions | Yield |
---|---|
Multistep reaction.; | 16% |
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
benzenesulfonyl chloride
Conditions | Yield |
---|---|
With tetra(n-butyl)ammonium hydrogensulfate In dichloromethane at 20℃; for 0.333333h; |
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
Conditions | Yield |
---|---|
With hydrogenchloride; n-butyllithium; N2; CO2 In tetrahydrofuran; diethyl ether |
[2-(5-methoxy-2-methyl-indol-3-yl)-ethyl]-dimethyl-amine
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