4-((R)-3-benzyloxy-1-dimethylcarbamoyl-propyl)-5-oxo-[1,4]diazepane-1-carboxylic acid benzyl ester

Base Information

Chemical Name:4-((R)-3-benzyloxy-1-dimethylcarbamoyl-propyl)-5-oxo-[1,4]diazepane-1-carboxylic acid benzyl ester
CAS No.:1290049-12-5
Molecular Formula:C₂₆H₃₃N₃O₅
Molecular Weight:467.565
Hs Code.:

Synonyms:4-((R)-3-benzyloxy-1-dimethylcarbamoyl-propyl)-5-oxo-[1,4]diazepane-1-carboxylic acid benzyl ester

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Chemical Property of 4-((R)-3-benzyloxy-1-dimethylcarbamoyl-propyl)-5-oxo-[1,4]diazepane-1-carboxylic acid benzyl ester

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Technology Process of 4-((R)-3-benzyloxy-1-dimethylcarbamoyl-propyl)-5-oxo-[1,4]diazepane-1-carboxylic acid benzyl ester

There total 7 articles about 4-((R)-3-benzyloxy-1-dimethylcarbamoyl-propyl)-5-oxo-[1,4]diazepane-1-carboxylic acid benzyl ester 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: 100.0%

: 1290049-11-4
Lithium (R)-4-benzyloxy-2-(4-benzyloxycarbonyl-7-oxo-[1,4]diazepan-1-yl)-butyrate

: 506-59-2
N,N-dimethylammonium chloride

: 1290049-12-5
4-((R)-3-benzyloxy-1-dimethylcarbamoyl-propyl)-5-oxo-[1,4]diazepane-1-carboxylic acid benzyl ester

Guidance literature:: With triethylamine; HATU; In N,N-dimethyl-formamide; at 0 - 20 ℃;

Reference yield:

: 13139-17-8
N-(Benzyloxycarbonyloxy)succinimide

: 1290049-12-5
4-((R)-3-benzyloxy-1-dimethylcarbamoyl-propyl)-5-oxo-[1,4]diazepane-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 7 steps

1.1: 18 h / 0 - 30 °C

1.2: 3 h / 0 - 20 °C

2.1: triethylamine; oxalyl dichloride; dimethyl sulfoxide / dichloromethane / -60 - -50 °C

3.1: triethylamine; acetic acid; borane pyridine / ethanol; 1,2-dichloro-ethane / 1.25 h / 20 °C

4.1: hydrogenchloride; water / 1,4-dioxane / 12 h / 10 - 20 °C

5.1: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 15 h / 0 - 20 °C

6.1: water; lithium hydroxide / tetrahydrofuran; methanol / 3 h / 0 °C

7.1: triethylamine; HATU / N,N-dimethyl-formamide / 0 - 20 °C

With hydrogenchloride; oxalyl dichloride; borane pyridine; water; acetic acid; dimethyl sulfoxide; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; HATU; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; dichloromethane; 1,2-dichloro-ethane; N,N-dimethyl-formamide;

Reference yield:

: 1205542-41-1
3-[benzyloxycarbonyl-(2-oxo-ethyl)-amino]-propionic acid tert-butyl ester

: 1290049-12-5
4-((R)-3-benzyloxy-1-dimethylcarbamoyl-propyl)-5-oxo-[1,4]diazepane-1-carboxylic acid benzyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine; acetic acid; borane pyridine / ethanol; 1,2-dichloro-ethane / 1.25 h / 20 °C

2: hydrogenchloride; water / 1,4-dioxane / 12 h / 10 - 20 °C

3: triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 15 h / 0 - 20 °C

4: water; lithium hydroxide / tetrahydrofuran; methanol / 3 h / 0 °C

5: triethylamine; HATU / N,N-dimethyl-formamide / 0 - 20 °C

With hydrogenchloride; borane pyridine; water; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; HATU; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; dichloromethane; 1,2-dichloro-ethane; N,N-dimethyl-formamide;