tert-butyl (R)-1-(4-bromophenyl)-4-((R)-3-(7-chloro-1-(3-methoxypropyl)-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate

Base Information

Chemical Name:tert-butyl (R)-1-(4-bromophenyl)-4-((R)-3-(7-chloro-1-(3-methoxypropyl)-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate
CAS No.:1365884-67-8
Molecular Formula:C₃₁H₄₀BrClN₄O₄
Molecular Weight:648.04
Hs Code.:

Synonyms:tert-butyl (R)-1-(4-bromophenyl)-4-((R)-3-(7-chloro-1-(3-methoxypropyl)-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate

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Chemical Property of tert-butyl (R)-1-(4-bromophenyl)-4-((R)-3-(7-chloro-1-(3-methoxypropyl)-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate

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Technology Process of tert-butyl (R)-1-(4-bromophenyl)-4-((R)-3-(7-chloro-1-(3-methoxypropyl)-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate

There total 7 articles about tert-butyl (R)-1-(4-bromophenyl)-4-((R)-3-(7-chloro-1-(3-methoxypropyl)-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate 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:

: 1365884-63-4
(R)-tert-Butyl 3-(3-chloro-2-(3-methoxypropylamino)phen ylcarbamoyl)piperidine-1-carboxylate

: 1365884-67-8
tert-butyl (R)-1-(4-bromophenyl)-4-((R)-3-(7-chloro-1-(3-methoxypropyl)-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate

Guidance literature:: Multi-step reaction with 3 steps

1: acetic acid / 16 h / 70 °C / Inert atmosphere

2: trifluoroacetic acid / dichloromethane / 4 h / Inert atmosphere

3: 4-methyl-morpholine; HATU / N,N-dimethyl-formamide / 3 h / 20 °C / Inert atmosphere

With 4-methyl-morpholine; acetic acid; HATU; trifluoroacetic acid; In dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 59483-54-4
3-chloro-2-nitro-aniline

: 1365884-67-8
tert-butyl (R)-1-(4-bromophenyl)-4-((R)-3-(7-chloro-1-(3-methoxypropyl)-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate

Guidance literature:: Multi-step reaction with 4 steps

1.1: zinc; acetic acid / methanol / 20 °C / Cooling with ice

2.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; 4-methyl-morpholine / N,N-dimethyl-formamide / 20 °C

2.2: 3 h / 80 °C

3.1: trifluoroacetic acid / dichloromethane / 4 h / Inert atmosphere

4.1: 4-methyl-morpholine; HATU / N,N-dimethyl-formamide / 3 h / 20 °C / Inert atmosphere

With 4-methyl-morpholine; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; HATU; trifluoroacetic acid; zinc; In methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 2106-49-2
1-chloro-2-fluoro-3-nitrobenzene

: 1365884-67-8
tert-butyl (R)-1-(4-bromophenyl)-4-((R)-3-(7-chloro-1-(3-methoxypropyl)-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate

Guidance literature:: Multi-step reaction with 6 steps

1: triethylamine / dichloromethane / 0 - 20 °C / Inert atmosphere

2: zinc; acetic acid / methanol / 16 h / 20 °C / Inert atmosphere

3: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 16 h / 20 °C / Inert atmosphere

4: acetic acid / 16 h / 70 °C / Inert atmosphere

5: trifluoroacetic acid / dichloromethane / 4 h / Inert atmosphere

6: 4-methyl-morpholine; HATU / N,N-dimethyl-formamide / 3 h / 20 °C / Inert atmosphere

With 4-methyl-morpholine; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; HATU; trifluoroacetic acid; zinc; In methanol; dichloromethane; N,N-dimethyl-formamide;