(R)-N-(2-chloro-4-methylphenyl)-2-((1-(2-((4-methylpiperazin-1-yl)methyl)phenyl)-1H-benzo[d]imidazol-2-yl)thio)propanamide

Base Information

Chemical Name:(R)-N-(2-chloro-4-methylphenyl)-2-((1-(2-((4-methylpiperazin-1-yl)methyl)phenyl)-1H-benzo[d]imidazol-2-yl)thio)propanamide
CAS No.:1401791-45-4
Molecular Formula:C₂₉H₃₂ClN₅OS
Molecular Weight:534.125
Hs Code.:

Synonyms:(R)-N-(2-chloro-4-methylphenyl)-2-((1-(2-((4-methylpiperazin-1-yl)methyl)phenyl)-1H-benzo[d]imidazol-2-yl)thio)propanamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (R)-N-(2-chloro-4-methylphenyl)-2-((1-(2-((4-methylpiperazin-1-yl)methyl)phenyl)-1H-benzo[d]imidazol-2-yl)thio)propanamide

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Technology Process of (R)-N-(2-chloro-4-methylphenyl)-2-((1-(2-((4-methylpiperazin-1-yl)methyl)phenyl)-1H-benzo[d]imidazol-2-yl)thio)propanamide

There total 8 articles about (R)-N-(2-chloro-4-methylphenyl)-2-((1-(2-((4-methylpiperazin-1-yl)methyl)phenyl)-1H-benzo[d]imidazol-2-yl)thio)propanamide 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: 92.0%

: 1429642-79-4
(S)-2-bromo-N-(2-chloro-4-methylphenyl)propanamide

: 1429642-76-1
1-(2-((4-methylpiperazin-1-yl)methyl)phenyl)-1H-benzo[d]imidazole-2-thiol

: 1401791-45-4
(R)-N-(2-chloro-4-methylphenyl)-2-((1-(2-((4-methylpiperazin-1-yl)methyl)phenyl)-1H-benzo[d]imidazol-2-yl)thio)propanamide

Guidance literature:: 1-(2-((4-methylpiperazin-1-yl)methyl)phenyl)-1H-benzo[d]imidazole-2-thiol; With potassium carbonate; In methanol; at 45 ℃; for 2h; Sonication;

(S)-2-bromo-N-(2-chloro-4-methylphenyl)propanamide; In N,N-dimethyl-formamide; at 0 ℃; for 1h;
DOI:10.3762/bjoc.9.23

Reference yield:

: N-(2-((4-methylpiperazin-1-yl)methyl)phenyl)benzene-1,2-diamine

: 1401791-45-4
(R)-N-(2-chloro-4-methylphenyl)-2-((1-(2-((4-methylpiperazin-1-yl)methyl)phenyl)-1H-benzo[d]imidazol-2-yl)thio)propanamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: dichloromethane / 1 h / 20 °C

2.1: potassium carbonate / methanol / 2 h / 45 °C / Sonication

2.2: 1 h / 0 °C

With potassium carbonate; In methanol; dichloromethane;
DOI:10.3762/bjoc.9.23

Reference yield:

: 552-89-6
2-nitro-benzaldehyde

: 1401791-45-4
(R)-N-(2-chloro-4-methylphenyl)-2-((1-(2-((4-methylpiperazin-1-yl)methyl)phenyl)-1H-benzo[d]imidazol-2-yl)thio)propanamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 18 h / 20 °C

2.1: hydrogen / ethanol / 1 h / 20 °C / 2068.65 Torr

3.1: triethylamine / 2 h / 160 °C / Sealed tube

4.1: hydrogen; palladium 10% on activated carbon / ethanol / 20 °C / 2585.81 Torr

5.1: dichloromethane / 1 h / 20 °C

6.1: potassium carbonate / methanol / 2 h / 45 °C / Sonication

6.2: 1 h / 0 °C

With palladium 10% on activated carbon; hydrogen; sodium tris(acetoxy)borohydride; potassium carbonate; acetic acid; triethylamine; In methanol; ethanol; dichloromethane;
DOI:10.3762/bjoc.9.23