tert-butyl (R)-1-(4-bromophenyl)-4-((R)-3-(3-(3-methoxypropyl)-3H-imidazo[4,5-c]pyridin-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate

Base Information

Chemical Name:tert-butyl (R)-1-(4-bromophenyl)-4-((R)-3-(3-(3-methoxypropyl)-3H-imidazo[4,5-c]pyridin-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate
CAS No.:1365884-89-4
Molecular Formula:C₃₀H₄₀BrN₅O₄
Molecular Weight:614.583
Hs Code.:

Synonyms:tert-butyl (R)-1-(4-bromophenyl)-4-((R)-3-(3-(3-methoxypropyl)-3H-imidazo[4,5-c]pyridin-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-(3-(3-methoxypropyl)-3H-imidazo[4,5-c]pyridin-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-(3-(3-methoxypropyl)-3H-imidazo[4,5-c]pyridin-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate

There total 6 articles about tert-butyl (R)-1-(4-bromophenyl)-4-((R)-3-(3-(3-methoxypropyl)-3H-imidazo[4,5-c]pyridin-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: 85.0%

: 331763-75-8
(R)-4-(4-bromophenyl)-3-((tert-butoxycarbonyl)amino)butanoic acid

: 1365884-88-3
(R)-3-(3-Methoxypropyl)-2-(piperidin-3-yl)-3H-imidazo[4,5-c]pyridine

: 1365884-89-4
tert-butyl (R)-1-(4-bromophenyl)-4-((R)-3-(3-(3-methoxypropyl)-3H-imidazo[4,5-c]pyridin-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate

Guidance literature:: With 4-methyl-morpholine; HATU; In N,N-dimethyl-formamide; at 20 ℃; for 3h; Inert atmosphere;

Reference yield:

: 1678-49-5
3-Bromo-4-nitropyridine N-oxide

: 1365884-89-4
tert-butyl (R)-1-(4-bromophenyl)-4-((R)-3-(3-(3-methoxypropyl)-3H-imidazo[4,5-c]pyridin-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate

Guidance literature:: Multi-step reaction with 6 steps

1: potassium carbonate / acetonitrile / 0 - 20 °C / Inert atmosphere

2: hydrogen / Ranay Ni / methanol / 16 h

3: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; 4-methyl-morpholine / N,N-dimethyl-formamide / 16 h / 20 °C / Inert atmosphere

4: acetic acid / 1.5 h / 85 °C / Microwave irradiation

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; hydrogen; potassium carbonate; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; HATU; trifluoroacetic acid; Ranay Ni; In methanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1365884-84-9
3-(3-methoxypropylamino)-4-nitropyridine 1-oxide

: 1365884-89-4
tert-butyl (R)-1-(4-bromophenyl)-4-((R)-3-(3-(3-methoxypropyl)-3H-imidazo[4,5-c]pyridin-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate

Guidance literature:: Multi-step reaction with 5 steps

1: hydrogen / Ranay Ni / methanol / 16 h

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; 4-methyl-morpholine / N,N-dimethyl-formamide / 16 h / 20 °C / Inert atmosphere

3: acetic acid / 1.5 h / 85 °C / Microwave irradiation

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

5: 4-methyl-morpholine; HATU / N,N-dimethyl-formamide / 3 h / 20 °C / Inert atmosphere

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