[4-chloro-2-[(4-chloro-2-methoxy-6-methylphenyl)amino]-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]acetic acid

Base Information

Chemical Name:[4-chloro-2-[(4-chloro-2-methoxy-6-methylphenyl)amino]-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]acetic acid
CAS No.:913299-14-6
Molecular Formula:C₂₂H₂₅Cl₂N₃O₃
Molecular Weight:450.365
Hs Code.:

Synonyms:[4-chloro-2-[(4-chloro-2-methoxy-6-methylphenyl)amino]-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]acetic acid

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Chemical Property of [4-chloro-2-[(4-chloro-2-methoxy-6-methylphenyl)amino]-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]acetic acid

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Technology Process of [4-chloro-2-[(4-chloro-2-methoxy-6-methylphenyl)amino]-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]acetic acid

There total 8 articles about [4-chloro-2-[(4-chloro-2-methoxy-6-methylphenyl)amino]-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]acetic acid 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: 99.1%

: 913299-04-4
isopropyl [4-chloro-2-[(4-chloro-2-methoxy-6-methylphenyl)amino]-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]acetate

: 913299-14-6
[4-chloro-2-[(4-chloro-2-methoxy-6-methylphenyl)amino]-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]acetic acid

Guidance literature:: isopropyl [4-chloro-2-[(4-chloro-2-methoxy-6-methylphenyl)amino]-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]acetate; With water; sodium hydroxide; In methanol; at 20 ℃; for 15h;

With hydrogenchloride; In methanol; water;

Reference yield:

: 913299-06-6
4-[(E/Z)-1-ethylprop-1-en-1-yl]-1,3-dihydro-2H-benzimidazol-2-one

: 913299-14-6
[4-chloro-2-[(4-chloro-2-methoxy-6-methylphenyl)amino]-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]acetic acid

Guidance literature:: Multi-step reaction with 8 steps

1: ammonium formate / palladium 10% on activated carbon / ethanol / 15 h / 20 °C

2: dmap / 1,2-dichloro-ethane / 0.5 h / 0 °C

3: potassium carbonate / N,N-dimethyl-formamide / 5 h / 20 °C

4: hydrogenchloride / ethyl acetate / 1 h / 20 °C

5: N-chloro-succinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 72 h / 70 °C

6: trichlorophosphate / 48 h / 100 °C

7: 1-methyl-pyrrolidin-2-one / 108 h / 110 °C

8: methanol; sodium hydroxide; water / 15 h / 20 °C

With hydrogenchloride; methanol; dmap; sodium hydroxide; N-chloro-succinimide; 2,2'-azobis(isobutyronitrile); water; ammonium formate; potassium carbonate; trichlorophosphate; palladium 10% on activated carbon; In 1-methyl-pyrrolidin-2-one; tetrachloromethane; ethanol; ethyl acetate; 1,2-dichloro-ethane; N,N-dimethyl-formamide;

Reference yield:

: isopropyl [2,4-dichloro-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]acetate

: 913299-14-6
[4-chloro-2-[(4-chloro-2-methoxy-6-methylphenyl)amino]-7-(1-ethylpropyl)-1H-benzimidazol-1-yl]acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: 1-methyl-pyrrolidin-2-one / 108 h / 110 °C

2: methanol; sodium hydroxide; water / 15 h / 20 °C

With methanol; sodium hydroxide; water; In 1-methyl-pyrrolidin-2-one;