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formaldehyd
dimethyl amine
6-bromo-5-hydroxy-1-methyl-2-phenylthiomethylindole-3-carboxylic acid ethyl ester
Arbidol hydrochloride
Conditions | Yield |
---|---|
Stage #1: formaldehyd; dimethyl amine; 6-bromo-5-hydroxy-1-methyl-2-phenylthiomethylindole-3-carboxylic acid ethyl ester With aminosulfonic acid In water at 30 - 40℃; for 3h; Cooling with ice; Stage #2: With hydrogenchloride In water; acetone at 60℃; pH=1; | 85.6% |
arbidol
Arbidol hydrochloride
Conditions | Yield |
---|---|
With hydrogenchloride In acetone for 0.5h; Reflux; | 75% |
Arbidol hydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: potassium carbonate; palladium diacetate; copper diacetate / N,N-dimethyl-formamide / 3 h / 80 °C 2.1: potassium carbonate / N,N-dimethyl-formamide / 6 h / 100 °C 3.1: dibenzoyl peroxide; bromine / chloroform / 3 h / Reflux 4.1: sodium hydroxide / methanol / 2 h 4.2: 3 h 5.1: aminosulfonic acid / water / 3 h / 30 - 40 °C / Cooling with ice 5.2: 60 °C / pH 1 View Scheme |
ethyl 5-acetyloxy-2-methyl-1H-indole-3-carboxylate
Arbidol hydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 4 steps 1.1: potassium carbonate / N,N-dimethyl-formamide / 6 h / 100 °C 2.1: dibenzoyl peroxide; bromine / chloroform / 3 h / Reflux 3.1: sodium hydroxide / methanol / 2 h 3.2: 3 h 4.1: aminosulfonic acid / water / 3 h / 30 - 40 °C / Cooling with ice 4.2: 60 °C / pH 1 View Scheme |
1,2-dimethyl-5-acetoxy-1H-indole-3-carboxylic acid ethyl ester
Arbidol hydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: dibenzoyl peroxide; bromine / chloroform / 3 h / Reflux 2.1: sodium hydroxide / methanol / 2 h 2.2: 3 h 3.1: aminosulfonic acid / water / 3 h / 30 - 40 °C / Cooling with ice 3.2: 60 °C / pH 1 View Scheme | |
Multi-step reaction with 4 steps 1.1: [RhCl2(p-cymene)]2; N-Bromosuccinimide / water; N,N-dimethyl acetamide / 24 h / 90 °C / Inert atmosphere 2.1: potassium hydroxide; methanol / 0.25 h / 20 °C 2.2: 4 h / 20 °C 3.1: acetic acid / water / 0.25 h / 0 °C 3.2: 4 h / 80 °C 4.1: hydrogenchloride / acetone / 0.5 h / Reflux View Scheme |
4-nitro-phenol
Arbidol hydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 8 steps 1.1: pyridine / acetone / 4 h / 20 °C / Reflux 2.1: iron; ammonium chloride / ethanol; water / 2 h / Reflux 3.1: indium(III) bromide / dichloromethane / 3 h / Reflux 4.1: potassium carbonate; palladium diacetate; copper diacetate / N,N-dimethyl-formamide / 3 h / 80 °C 5.1: potassium carbonate / N,N-dimethyl-formamide / 6 h / 100 °C 6.1: dibenzoyl peroxide; bromine / chloroform / 3 h / Reflux 7.1: sodium hydroxide / methanol / 2 h 7.2: 3 h 8.1: aminosulfonic acid / water / 3 h / 30 - 40 °C / Cooling with ice 8.2: 60 °C / pH 1 View Scheme |
4-nitrophenol acetate
Arbidol hydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 7 steps 1.1: iron; ammonium chloride / ethanol; water / 2 h / Reflux 2.1: indium(III) bromide / dichloromethane / 3 h / Reflux 3.1: potassium carbonate; palladium diacetate; copper diacetate / N,N-dimethyl-formamide / 3 h / 80 °C 4.1: potassium carbonate / N,N-dimethyl-formamide / 6 h / 100 °C 5.1: dibenzoyl peroxide; bromine / chloroform / 3 h / Reflux 6.1: sodium hydroxide / methanol / 2 h 6.2: 3 h 7.1: aminosulfonic acid / water / 3 h / 30 - 40 °C / Cooling with ice 7.2: 60 °C / pH 1 View Scheme |
p-aminophenyl acetate
Arbidol hydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 6 steps 1.1: indium(III) bromide / dichloromethane / 3 h / Reflux 2.1: potassium carbonate; palladium diacetate; copper diacetate / N,N-dimethyl-formamide / 3 h / 80 °C 3.1: potassium carbonate / N,N-dimethyl-formamide / 6 h / 100 °C 4.1: dibenzoyl peroxide; bromine / chloroform / 3 h / Reflux 5.1: sodium hydroxide / methanol / 2 h 5.2: 3 h 6.1: aminosulfonic acid / water / 3 h / 30 - 40 °C / Cooling with ice 6.2: 60 °C / pH 1 View Scheme |
mecarbinate
Arbidol hydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 5 steps 1.1: 4 h / Reflux 2.1: [RhCl2(p-cymene)]2; N-Bromosuccinimide / water; N,N-dimethyl acetamide / 24 h / 90 °C / Inert atmosphere 3.1: potassium hydroxide; methanol / 0.25 h / 20 °C 3.2: 4 h / 20 °C 4.1: acetic acid / water / 0.25 h / 0 °C 4.2: 4 h / 80 °C 5.1: hydrogenchloride / acetone / 0.5 h / Reflux View Scheme |
5-acetoxy-6-bromo-2-bromomethyl-1-methylindole-3-carboxylic acid ethyl ester
Arbidol hydrochloride
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1.1: potassium hydroxide; methanol / 0.25 h / 20 °C 1.2: 4 h / 20 °C 2.1: acetic acid / water / 0.25 h / 0 °C 2.2: 4 h / 80 °C 3.1: hydrogenchloride / acetone / 0.5 h / Reflux View Scheme |
Conditions | Yield |
---|---|
Stage #1: Arbidol hydrochloride With sodium hydroxide In water Stage #2: maleic acid In ethyl acetate |
Conditions | Yield |
---|---|
Stage #1: Arbidol hydrochloride With sodium hydroxide In water Stage #2: salicylic acid In ethyl acetate |
2,5-dihydroxybenzoic acid.
Arbidol hydrochloride
umifenovir gentisate
Conditions | Yield |
---|---|
Stage #1: Arbidol hydrochloride With sodium hydroxide In water Stage #2: 2,5-dihydroxybenzoic acid. In ethyl acetate |
1,5-pentanedioic acid
Arbidol hydrochloride
umifenovir hydrogen glutarate
Conditions | Yield |
---|---|
Stage #1: Arbidol hydrochloride With sodium hydroxide In water Stage #2: 1,5-pentanedioic acid In ethyl acetate |
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