N-cyclopropyl-4-{6-[(1RS)-1-(3-fluoro-4-methoxyphenyl)ethyl]-4-[(3,3,3-trifluoropropyl)amino]-1H-benzimidazol-1-yl}-2-methylbenzamide

Base Information

Chemical Name:N-cyclopropyl-4-{6-[(1RS)-1-(3-fluoro-4-methoxyphenyl)ethyl]-4-[(3,3,3-trifluoropropyl)amino]-1H-benzimidazol-1-yl}-2-methylbenzamide
CAS No.:1401450-94-9
Molecular Formula:C₃₀H₃₀F₄N₄O₂
Molecular Weight:554.587
Hs Code.:

Synonyms:N-cyclopropyl-4-{6-[(1RS)-1-(3-fluoro-4-methoxyphenyl)ethyl]-4-[(3,3,3-trifluoropropyl)amino]-1H-benzimidazol-1-yl}-2-methylbenzamide

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Chemical Property of N-cyclopropyl-4-{6-[(1RS)-1-(3-fluoro-4-methoxyphenyl)ethyl]-4-[(3,3,3-trifluoropropyl)amino]-1H-benzimidazol-1-yl}-2-methylbenzamide

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Technology Process of N-cyclopropyl-4-{6-[(1RS)-1-(3-fluoro-4-methoxyphenyl)ethyl]-4-[(3,3,3-trifluoropropyl)amino]-1H-benzimidazol-1-yl}-2-methylbenzamide

There total 12 articles about N-cyclopropyl-4-{6-[(1RS)-1-(3-fluoro-4-methoxyphenyl)ethyl]-4-[(3,3,3-trifluoropropyl)amino]-1H-benzimidazol-1-yl}-2-methylbenzamide 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: 46.0%

: 1401450-93-8
N-cyclopropyl-4-{6-[1-(3-fluoro-4-methoxyphenyl)vinyl]-4-[(3,3,3-trifluoropropyl)amino]-1H-benzimidazol-1-yl}-2-methylbenzamide

: 1401450-94-9
N-cyclopropyl-4-{6-[(1RS)-1-(3-fluoro-4-methoxyphenyl)ethyl]-4-[(3,3,3-trifluoropropyl)amino]-1H-benzimidazol-1-yl}-2-methylbenzamide

Guidance literature:: With hydrogen; palladium 10% on activated carbon; In ethanol; at 23 ℃; for 48h;

Reference yield:

: 1121586-23-9
5-bromobenzene-1,2,3-triamine

: 1401450-94-9
N-cyclopropyl-4-{6-[(1RS)-1-(3-fluoro-4-methoxyphenyl)ethyl]-4-[(3,3,3-trifluoropropyl)amino]-1H-benzimidazol-1-yl}-2-methylbenzamide

Guidance literature:: Multi-step reaction with 8 steps

1.1: hydrogenchloride / 20 °C / Reflux

1.2: pH 8

2.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 23 °C

2.2: 3 °C

3.1: pyridine N-oxide; pyridine; copper diacetate / dichloromethane / 60 h / 23 °C

4.1: N-ethyl-N,N-diisopropylamine; palladium diacetate; catacxium A / toluene / 100 °C / 10501.1 Torr

5.1: water; lithium hydroxide / tetrahydrofuran; methanol / 23 °C

6.1: dmap; HATU / N,N-dimethyl-formamide / 23 °C

7.1: n-butyllithium / hexane; tetrahydrofuran / 0.5 h / 23 °C

7.2: 23 °C

8.1: hydrogen / palladium 10% on activated carbon / ethanol / 48 h / 23 °C

With pyridine; pyridine N-oxide; hydrogenchloride; dmap; n-butyllithium; water; hydrogen; copper diacetate; palladium diacetate; sodium tris(acetoxy)borohydride; acetic acid; N-ethyl-N,N-diisopropylamine; HATU; lithium hydroxide; catacxium A; palladium 10% on activated carbon; In tetrahydrofuran; methanol; ethanol; hexane; dichloromethane; N,N-dimethyl-formamide; toluene;

Reference yield:

: 1360899-50-8
6-bromo-1H-1,3-benzodiazol-4-amine

: 1401450-94-9
N-cyclopropyl-4-{6-[(1RS)-1-(3-fluoro-4-methoxyphenyl)ethyl]-4-[(3,3,3-trifluoropropyl)amino]-1H-benzimidazol-1-yl}-2-methylbenzamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: acetic acid; sodium tris(acetoxy)borohydride / dichloromethane / 23 °C

1.2: 3 °C

2.1: pyridine N-oxide; pyridine; copper diacetate / dichloromethane / 60 h / 23 °C

3.1: N-ethyl-N,N-diisopropylamine; palladium diacetate; catacxium A / toluene / 100 °C / 10501.1 Torr

4.1: water; lithium hydroxide / tetrahydrofuran; methanol / 23 °C

5.1: dmap; HATU / N,N-dimethyl-formamide / 23 °C

6.1: n-butyllithium / hexane; tetrahydrofuran / 0.5 h / 23 °C

6.2: 23 °C

7.1: hydrogen / palladium 10% on activated carbon / ethanol / 48 h / 23 °C

With pyridine; pyridine N-oxide; dmap; n-butyllithium; water; hydrogen; copper diacetate; palladium diacetate; sodium tris(acetoxy)borohydride; acetic acid; N-ethyl-N,N-diisopropylamine; HATU; lithium hydroxide; catacxium A; palladium 10% on activated carbon; In tetrahydrofuran; methanol; ethanol; hexane; dichloromethane; N,N-dimethyl-formamide; toluene;