2-(4-aminophenylimino)-5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methylthiazolidin-4-one

Base Information

Chemical Name:2-(4-aminophenylimino)-5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methylthiazolidin-4-one
CAS No.:1186634-19-4
Molecular Formula:C₃₀H₃₁N₃O₂S
Molecular Weight:497.661
Hs Code.:

Synonyms:2-(4-aminophenylimino)-5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methylthiazolidin-4-one

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Chemical Property of 2-(4-aminophenylimino)-5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methylthiazolidin-4-one

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Technology Process of 2-(4-aminophenylimino)-5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methylthiazolidin-4-one

There total 7 articles about 2-(4-aminophenylimino)-5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methylthiazolidin-4-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 74.0%

: 1186634-18-3
5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methyl-2-(4-nitrophenyimino)thiazolidin-4-one

: 1186634-19-4
2-(4-aminophenylimino)-5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methylthiazolidin-4-one

Guidance literature:: With iron; acetic acid; at 20 ℃; for 6h;

Reference yield:

: 63500-84-5
3-methyl-2-(4-nitro-phenylimino)-thiazolidin-4-one

: 1186634-19-4
2-(4-aminophenylimino)-5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methylthiazolidin-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: piperidine / ethanol / 14 h / Reflux

2: iron; acetic acid / 6 h / 20 °C

With piperidine; iron; acetic acid; In ethanol;

Reference yield:

: 20029-52-1
4-cyclohexylbenzoic acid

: 1186634-19-4
2-(4-aminophenylimino)-5-(4-(4-cyclohexylbenzyloxy)benzylidene)-3-methylthiazolidin-4-one

Guidance literature:: Multi-step reaction with 6 steps

1.1: sulfuric acid / 5 h / Reflux

2.1: lithium aluminium tetrahydride / tetrahydrofuran / 2 h / 0 °C

2.2: 0 °C

3.1: thionyl chloride / dichloromethane / 0.5 h / 0 °C

4.1: potassium carbonate / N,N-dimethyl-formamide / 20 - 60 °C

5.1: piperidine / ethanol / 14 h / Reflux

6.1: iron; acetic acid / 6 h / 20 °C

With piperidine; lithium aluminium tetrahydride; thionyl chloride; sulfuric acid; iron; potassium carbonate; acetic acid; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;