(1-(2-(4-bromophenyl)-2-oxoethylcarbamoyl)cyclopropyl)carbamic acid tert-butyl ester

Base Information

Chemical Name:(1-(2-(4-bromophenyl)-2-oxoethylcarbamoyl)cyclopropyl)carbamic acid tert-butyl ester
CAS No.:1256386-68-1
Molecular Formula:C₁₇H₂₁BrN₂O₄
Molecular Weight:397.269
Hs Code.:

Synonyms:(1-(2-(4-bromophenyl)-2-oxoethylcarbamoyl)cyclopropyl)carbamic acid tert-butyl ester

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Chemical Property of (1-(2-(4-bromophenyl)-2-oxoethylcarbamoyl)cyclopropyl)carbamic acid tert-butyl ester

Chemical Property:

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Technology Process of (1-(2-(4-bromophenyl)-2-oxoethylcarbamoyl)cyclopropyl)carbamic acid tert-butyl ester

There total 1 articles about (1-(2-(4-bromophenyl)-2-oxoethylcarbamoyl)cyclopropyl)carbamic acid tert-butyl 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: 90.0%

: 5467-72-1
α-amino-4-bromoacetophenone hydrochloride

: 88950-64-5
1-<(tert-butyloxy)carbonylamino>cyclopropane-1-carboxylic acid

: 1256386-68-1
(1-(2-(4-bromophenyl)-2-oxoethylcarbamoyl)cyclopropyl)carbamic acid tert-butyl ester

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; for 18h;

Reference yield:

: 1256386-68-1
(1-(2-(4-bromophenyl)-2-oxoethylcarbamoyl)cyclopropyl)carbamic acid tert-butyl ester

: 1256386-67-0
(1-(5-(4-bromophenyl)-1H-imidazol-2-yl)cyclopropyl)carbamic acid tert-butyl ester

Guidance literature:: With ammonium acetate; In xylene; at 130 ℃; for 18h; Sealed tube;

Reference yield:

: 1256386-68-1
(1-(2-(4-bromophenyl)-2-oxoethylcarbamoyl)cyclopropyl)carbamic acid tert-butyl ester

2-methyl-1-(1-(1-(5-(4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl)-1H-imidazol-2-yl)cyclopropylcarbamoyl)propyl)carbamic acid methyl ester: 1256386-70-5
2-methyl-1-(1-(1-(5-(4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)phenyl)-1H-imidazol-2-yl)cyclopropylcarbamoyl)propyl)carbamic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: ammonium acetate / xylene / 18 h / 130 °C / Sealed tube

2.1: hydrogenchloride / 1,4-dioxane / 2 h

2.2: 18 h

3.1: potassium acetate / tetrakis(triphenylphosphine) palladium⁽⁰⁾ / 1,4-dioxane / 18 h / 80 °C / Sealed tube

With hydrogenchloride; ammonium acetate; potassium acetate; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In 1,4-dioxane; xylene;