(E)-N-(6-((1,1-dioxidothiomorpholino)methyl)-1-((1s,4s)-4-(isopropylcarbamoyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)ylidene)-4-fluorobenzamide

Base Information

Chemical Name:(E)-N-(6-((1,1-dioxidothiomorpholino)methyl)-1-((1s,4s)-4-(isopropylcarbamoyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)ylidene)-4-fluorobenzamide
CAS No.:1357921-10-8
Molecular Formula:C₂₉H₃₆FN₅O₄S
Molecular Weight:569.7
Hs Code.:

(E)-N-(6-((1,1-dioxidothiomorpholino)methyl)-1-((1s,4s)-4-(isopropylcarbamoyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)ylidene)-4-fluorobenzamide

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Chemical Property of (E)-N-(6-((1,1-dioxidothiomorpholino)methyl)-1-((1s,4s)-4-(isopropylcarbamoyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)ylidene)-4-fluorobenzamide

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Technology Process of (E)-N-(6-((1,1-dioxidothiomorpholino)methyl)-1-((1s,4s)-4-(isopropylcarbamoyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)ylidene)-4-fluorobenzamide

There total 5 articles about (E)-N-(6-((1,1-dioxidothiomorpholino)methyl)-1-((1s,4s)-4-(isopropylcarbamoyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)ylidene)-4-fluorobenzamide 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:

: 503315-74-0
(3-fluoro-4-nitrophenyl)methanol

: 1357921-10-8,1388225-62-4
(E)-N-(6-((1,1-dioxidothiomorpholino)methyl)-1-((1s,4s)-4-(isopropylcarbamoyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)ylidene)-4-fluorobenzamide

Guidance literature:: Multi-step reaction with 5 steps

1: N-ethyl-N,N-diisopropylamine / acetonitrile / 16 h / 80 °C

2: palladium 10% on activated carbon; hydrogen / ethanol

3: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 2 h / 0 - 60 °C

4: thionyl chloride / dichloromethane / 0.5 h / 0 - 20 °C

5: acetonitrile / 16 h / 0 - 20 °C

With thionyl chloride; palladium 10% on activated carbon; hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; ethanol; dichloromethane; acetonitrile;
DOI:10.1021/jm3005866

Reference yield:

: 1357920-83-2,1388225-59-9
(E)-4-fluoro-N-(6-(hydroxymethyl)-1-( (1s,4s)-4-(isopropylcarbamoyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)-ylidene)benzamide

: 1357921-10-8,1388225-62-4
(E)-N-(6-((1,1-dioxidothiomorpholino)methyl)-1-((1s,4s)-4-(isopropylcarbamoyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)ylidene)-4-fluorobenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / dichloromethane / 0.5 h / 0 - 20 °C

2: acetonitrile / 16 h / 0 - 20 °C

With thionyl chloride; In dichloromethane; acetonitrile;
DOI:10.1021/jm3005866

Reference yield:

: 403-43-0
4-fluorobenzoyl chloride

: 1357921-10-8,1388225-62-4
(E)-N-(6-((1,1-dioxidothiomorpholino)methyl)-1-((1s,4s)-4-(isopropylcarbamoyl)cyclohexyl)-1H-benzo[d]imidazol-2(3H)ylidene)-4-fluorobenzamide

Guidance literature:: Multi-step reaction with 4 steps

1: acetone / 7 h / 50 °C

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 2 h / 0 - 60 °C

3: thionyl chloride / dichloromethane / 0.5 h / 0 - 20 °C

4: acetonitrile / 16 h / 0 - 20 °C

With thionyl chloride; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane; acetone; acetonitrile;
DOI:10.1021/jm3005866