4-(6-chloro-3-(2-(dipropylamino)-2-oxoethyl)imidazo[1,2-a]pyridin-2-yl)phenyl-3,4-dihydroxyphenethylcarbamate

Base Information

Chemical Name:4-(6-chloro-3-(2-(dipropylamino)-2-oxoethyl)imidazo[1,2-a]pyridin-2-yl)phenyl-3,4-dihydroxyphenethylcarbamate
CAS No.:1402402-86-1
Molecular Formula:C₃₀H₃₃ClN₄O₅
Molecular Weight:565.069
Hs Code.:

Synonyms:4-(6-chloro-3-(2-(dipropylamino)-2-oxoethyl)imidazo[1,2-a]pyridin-2-yl)phenyl-3,4-dihydroxyphenethylcarbamate

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Chemical Property of 4-(6-chloro-3-(2-(dipropylamino)-2-oxoethyl)imidazo[1,2-a]pyridin-2-yl)phenyl-3,4-dihydroxyphenethylcarbamate

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Technology Process of 4-(6-chloro-3-(2-(dipropylamino)-2-oxoethyl)imidazo[1,2-a]pyridin-2-yl)phenyl-3,4-dihydroxyphenethylcarbamate

There total 4 articles about 4-(6-chloro-3-(2-(dipropylamino)-2-oxoethyl)imidazo[1,2-a]pyridin-2-yl)phenyl-3,4-dihydroxyphenethylcarbamate 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:

: 1402402-90-7
4-(6-chloro-3-(2-(dipropylamino)-2-oxoethyl)imidazo[1,2-a]pyridin-2-yl)phenyl 4-nitrophenyl carbonate

: 62-31-7
dopamine hydrochloride

: 1402402-86-1
4-(6-chloro-3-(2-(dipropylamino)-2-oxoethyl)imidazo[1,2-a]pyridin-2-yl)phenyl-3,4-dihydroxyphenethylcarbamate

Guidance literature:: In tetrahydrofuran; N,N-dimethyl-formamide; at 20 ℃; for 12h; Inert atmosphere;
DOI:10.1016/j.ijpharm.2012.08.023

Reference yield:

: 1072-98-6
5-chloro-2-pyridylamine

: 1402402-86-1
4-(6-chloro-3-(2-(dipropylamino)-2-oxoethyl)imidazo[1,2-a]pyridin-2-yl)phenyl-3,4-dihydroxyphenethylcarbamate

Guidance literature:: Multi-step reaction with 6 steps

1: butan-1-ol / Inert atmosphere; Reflux

2: water; sodium hydroxide / butan-1-ol / 50 °C / Inert atmosphere

3: hydrogen bromide / Inert atmosphere; Reflux

4: triethylamine; 1,1'-carbonyldiimidazole / tetrahydrofuran; N,N-dimethyl-formamide / 20 °C / Inert atmosphere

5: triethylamine / tetrahydrofuran / 4 h / 50 °C / Inert atmosphere

6: tetrahydrofuran; N,N-dimethyl-formamide / 12 h / 20 °C / Inert atmosphere

With water; hydrogen bromide; triethylamine; 1,1'-carbonyldiimidazole; sodium hydroxide; In tetrahydrofuran; N,N-dimethyl-formamide; butan-1-ol;
DOI:10.1016/j.ijpharm.2012.08.023

Reference yield:

: 1073119-36-4
butyl 3-bromo-4-(4-methoxyphenyl)-4-oxobutanoate

: 1402402-86-1
4-(6-chloro-3-(2-(dipropylamino)-2-oxoethyl)imidazo[1,2-a]pyridin-2-yl)phenyl-3,4-dihydroxyphenethylcarbamate

Guidance literature:: Multi-step reaction with 6 steps

1: butan-1-ol / Inert atmosphere; Reflux

2: water; sodium hydroxide / butan-1-ol / 50 °C / Inert atmosphere

3: hydrogen bromide / Inert atmosphere; Reflux

4: triethylamine; 1,1'-carbonyldiimidazole / tetrahydrofuran; N,N-dimethyl-formamide / 20 °C / Inert atmosphere

5: triethylamine / tetrahydrofuran / 4 h / 50 °C / Inert atmosphere

6: tetrahydrofuran; N,N-dimethyl-formamide / 12 h / 20 °C / Inert atmosphere

With water; hydrogen bromide; triethylamine; 1,1'-carbonyldiimidazole; sodium hydroxide; In tetrahydrofuran; N,N-dimethyl-formamide; butan-1-ol;
DOI:10.1016/j.ijpharm.2012.08.023