{1-[4-(7-acetylamino-3-phenyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

Base Information

Chemical Name:{1-[4-(7-acetylamino-3-phenyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester
CAS No.:1356001-76-7
Molecular Formula:C₃₀H₃₂N₄O₃
Molecular Weight:496.609
Hs Code.:

Synonyms:{1-[4-(7-acetylamino-3-phenyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

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Chemical Property of {1-[4-(7-acetylamino-3-phenyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

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Technology Process of {1-[4-(7-acetylamino-3-phenyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

There total 5 articles about {1-[4-(7-acetylamino-3-phenyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-cyclobutyl}-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: 61.0%

: 1356001-74-5
{1-[4-(7-amino-3-phenyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

: 108-24-7
acetic anhydride

: 1356001-76-7
{1-[4-(7-acetylamino-3-phenyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

Guidance literature:: With pyridine; In dichloromethane; at 20 ℃; for 48h;

Reference yield:

: 1032349-98-6
tert-butyl 1-(4-(2-phenylacetyl)phenyl)cyclobutylcarbamate

: 1356001-76-7
{1-[4-(7-acetylamino-3-phenyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: pyridinium perbromide hydrobromide / tetrahydrofuran / 2 h / 20 °C

2: N-ethyl-N,N-diisopropylamine / ethanol / 4 h / Molecular sieve; Reflux

3: sodium hydroxide; water / methanol / 12 h / 20 °C

4: triethylamine; diphenyl phosphoryl azide / palladium 10% on activated carbon / N,N-dimethyl-formamide; water; methanol / 30 h / 20 - 100 °C

5: pyridine / dichloromethane / 48 h / 20 °C

With pyridine; pyridinium perbromide hydrobromide; diphenyl phosphoryl azide; water; triethylamine; N-ethyl-N,N-diisopropylamine; sodium hydroxide; palladium 10% on activated carbon; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 1356001-73-4
2-(4-(1-(tert-butoxycarbonylamino)cyclobutyl)phenyl)-3-phenylimidazo[1,2-a]pyridine-7-carboxylic acid

: 1356001-76-7
{1-[4-(7-acetylamino-3-phenyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine; diphenyl phosphoryl azide / palladium 10% on activated carbon / N,N-dimethyl-formamide; water; methanol / 30 h / 20 - 100 °C

2: pyridine / dichloromethane / 48 h / 20 °C

With pyridine; diphenyl phosphoryl azide; triethylamine; palladium 10% on activated carbon; In methanol; dichloromethane; water; N,N-dimethyl-formamide;