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

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Chemical Name:tert-butyl (R)-1-(4-(cyclohexylcarbamoyl)phenyl)-4-((R)-3-(1-(3-methoxypropyl)-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate
CAS No.:1365886-61-8
Molecular Formula:C₃₈H₅₃N₅O₅
Molecular Weight:659.869
Hs Code.:

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

There total 8 articles about tert-butyl (R)-1-(4-(cyclohexylcarbamoyl)phenyl)-4-((R)-3-(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: 39.0%

: 1365884-39-4
tert-butyl (R)-1-(4-bromophenyl)-4-((R)-3-(1-(3-methoxypropyl)-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate

: 108-91-8,157973-60-9
cyclohexylamine

: 13939-06-5,199620-15-0
molybdenum hexacarbonyl

: 1365886-61-8
tert-butyl (R)-1-(4-(cyclohexylcarbamoyl)phenyl)-4-((R)-3-(1-(3-methoxypropyl)-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate

Guidance literature:: With 1H-imidazole; 1,8-diazabicyclo[5.4.0]undec-7-ene; palladium diacetate; In tetrahydrofuran; at 150 ℃; for 0.25h; Microwave irradiation;

Reference yield:

: 163438-09-3
(R)-1-Boc-nipecotic acid

: 1365886-61-8
tert-butyl (R)-1-(4-(cyclohexylcarbamoyl)phenyl)-4-((R)-3-(1-(3-methoxypropyl)-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate

Guidance literature:: Multi-step reaction with 6 steps

1.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; 4-methyl-morpholine / N,N-dimethyl-formamide / 16 h / 20 °C / Inert atmosphere

2.1: acetic acid / 2 h / 65 °C / Inert atmosphere

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 °C / Inert atmosphere

3.2: 0 - 20 °C

4.1: hydrogenchloride; water / ethanol / 0.17 h / Inert atmosphere; Reflux

5.1: 4-methyl-morpholine; HATU / N,N-dimethyl-formamide / 20 °C

6.1: 1H-imidazole; 1,8-diazabicyclo[5.4.0]undec-7-ene / palladium diacetate / tetrahydrofuran / 0.25 h / 150 °C / Microwave irradiation

With 4-methyl-morpholine; 1H-imidazole; hydrogenchloride; water; sodium hydride; benzotriazol-1-ol; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; HATU; palladium diacetate; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; mineral oil;

Reference yield:

: 95-54-5
1,2-diamino-benzene

: 1365886-61-8
tert-butyl (R)-1-(4-(cyclohexylcarbamoyl)phenyl)-4-((R)-3-(1-(3-methoxypropyl)-1H-benzo[d]imidazol-2-yl)piperidin-1-yl)-4-oxobutan-2-ylcarbamate

Guidance literature:: Multi-step reaction with 6 steps

1.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; 4-methyl-morpholine / N,N-dimethyl-formamide / 16 h / 20 °C / Inert atmosphere

2.1: acetic acid / 2 h / 65 °C / Inert atmosphere

3.1: sodium hydride / N,N-dimethyl-formamide; mineral oil / 0.5 h / 0 °C / Inert atmosphere

3.2: 0 - 20 °C

4.1: hydrogenchloride; water / ethanol / 0.17 h / Inert atmosphere; Reflux

5.1: 4-methyl-morpholine; HATU / N,N-dimethyl-formamide / 20 °C

6.1: 1H-imidazole; 1,8-diazabicyclo[5.4.0]undec-7-ene / palladium diacetate / tetrahydrofuran / 0.25 h / 150 °C / Microwave irradiation

With 4-methyl-morpholine; 1H-imidazole; hydrogenchloride; water; sodium hydride; benzotriazol-1-ol; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; HATU; palladium diacetate; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; mineral oil;