2-tert-butoxycarbonylamino-5-(4-phenylethynylphenyI)imidazole-1-carboxylic acid tert-butyl ester

Base Information

• Chemical Name: 2-tert-butoxycarbonylamino-5-(4-phenylethynylphenyI)imidazole-1-carboxylic acid tert-butyl ester
• CAS No.: 1037183-86-0
• Molecular Formula: C₂₇H₂₉N₃O₄
• Molecular Weight: 459.545
• Mol file: 1037183-86-0.mol

Synonyms:2-tert-butoxycarbonylamino-5-(4-phenylethynylphenyI)imidazole-1-carboxylic acid tert-butyl ester

Chemical Property of 2-tert-butoxycarbonylamino-5-(4-phenylethynylphenyI)imidazole-1-carboxylic acid tert-butyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-tert-butoxycarbonylamino-5-(4-phenylethynylphenyI)imidazole-1-carboxylic acid tert-butyl ester

There total 1 articles about 2-tert-butoxycarbonylamino-5-(4-phenylethynylphenyI)imidazole-1-carboxylic 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%

2-tert-butoxycarbonylamino-5-(4-iodophenyl)imidazole-1-carboxylic acid tert-butyl ester (1037183-85-9) + phenylacetylene (536-74-3) → 2-tert-butoxycarbonylamino-5-(4-phenylethynylphenyI)imidazole-1-carboxylic acid tert-butyl ester (1037183-86-0)

Guidance literature:

With copper(l) iodide; N-ethyl-N,N-diisopropylamine; bis-triphenylphosphine-palladium(II) chloride; In tetrahydrofuran; at 20 ℃; for 12h;

DOI:10.1021/jo800618q

Reference yield:

2-tert-butoxycarbonylamino-5-(4-phenylethynylphenyI)imidazole-1-carboxylic acid tert-butyl ester (1037183-86-0) + trifluoroacetic acid (76-05-1) → 5-(4-phenylethynylphenyl)-1H-imidazol-2-ylamine trifluoroacetate

Guidance literature:

In dichloromethane; at 0 - 20 ℃;

Reference yield:

2-tert-butoxycarbonylamino-5-(4-phenylethynylphenyI)imidazole-1-carboxylic acid tert-butyl ester (1037183-86-0) → 5-(4-phenylethynylphenyl)-1H-imidazol-2-ylamine hydrochloride (1190333-08-4)

Guidance literature:

Multi-step reaction with 2 steps

1: dichloromethane / 0 - 20 °C

2: hydrogenchloride / diethyl ether; dichloromethane

With hydrogenchloride; In diethyl ether; dichloromethane;

upstream raw materials:

2-tert-butoxycarbonylamino-5-(4-iodophenyl)imidazole-1-carboxylic acid tert-butyl ester

phenylacetylene

Downstream raw materials:

5-(4-phenylethynylphenyl)-1H-imidazol-2-ylamine hydrochloride