N-(1-methylethyl)-2-[3-[3-(methyloxy)phenyl]-1-oxo-7-[4-(1-piperidinyl)-butyl]pyrrolo[1,2-a]pyrazin-2(1H)-yl]acetamide hydrochloride

Base Information

Chemical Name:N-(1-methylethyl)-2-[3-[3-(methyloxy)phenyl]-1-oxo-7-[4-(1-piperidinyl)-butyl]pyrrolo[1,2-a]pyrazin-2(1H)-yl]acetamide hydrochloride
CAS No.:1192682-83-9
Molecular Formula:C₂₈H₃₈N₄O₃*ClH
Molecular Weight:515.096
Hs Code.:

Synonyms:N-(1-methylethyl)-2-[3-[3-(methyloxy)phenyl]-1-oxo-7-[4-(1-piperidinyl)-butyl]pyrrolo[1,2-a]pyrazin-2(1H)-yl]acetamide hydrochloride

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Chemical Property of N-(1-methylethyl)-2-[3-[3-(methyloxy)phenyl]-1-oxo-7-[4-(1-piperidinyl)-butyl]pyrrolo[1,2-a]pyrazin-2(1H)-yl]acetamide hydrochloride

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Technology Process of N-(1-methylethyl)-2-[3-[3-(methyloxy)phenyl]-1-oxo-7-[4-(1-piperidinyl)-butyl]pyrrolo[1,2-a]pyrazin-2(1H)-yl]acetamide hydrochloride

There total 10 articles about N-(1-methylethyl)-2-[3-[3-(methyloxy)phenyl]-1-oxo-7-[4-(1-piperidinyl)-butyl]pyrrolo[1,2-a]pyrazin-2(1H)-yl]acetamide hydrochloride 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:

: 1192682-81-7
N-(1-methylethyl)-2-[3-[3-(methyloxy)phenyl]-1-oxo-7-[4-(1-piperidinyl)-butyl]pyrrolo[1,2-a]pyrazin-2(1H)-yl]acetamide

: 1192682-83-9
N-(1-methylethyl)-2-[3-[3-(methyloxy)phenyl]-1-oxo-7-[4-(1-piperidinyl)-butyl]pyrrolo[1,2-a]pyrazin-2(1H)-yl]acetamide hydrochloride

Guidance literature:: With hydrogenchloride; In diethyl ether; dichloromethane;

Reference yield:

: 110-89-4
piperidine

: 1192682-83-9
N-(1-methylethyl)-2-[3-[3-(methyloxy)phenyl]-1-oxo-7-[4-(1-piperidinyl)-butyl]pyrrolo[1,2-a]pyrazin-2(1H)-yl]acetamide hydrochloride

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate / acetonitrile / 8 h / 80 °C

2: hydrogen / palladium on activated charcoal / ethanol / 12 h / 20 °C / 760.05 Torr

3: hydrogenchloride / diethyl ether; dichloromethane

With hydrogenchloride; hydrogen; potassium carbonate; palladium on activated charcoal; In diethyl ether; ethanol; dichloromethane; acetonitrile;

Reference yield:

: 72652-33-6
4-iodo-2-(trichloroacetyl)pyrrole

: 1192682-83-9
N-(1-methylethyl)-2-[3-[3-(methyloxy)phenyl]-1-oxo-7-[4-(1-piperidinyl)-butyl]pyrrolo[1,2-a]pyrazin-2(1H)-yl]acetamide hydrochloride

Guidance literature:: Multi-step reaction with 8 steps

1.1: potassium carbonate / N,N-dimethyl-formamide / 6 h / 20 °C

2.1: ammonium acetate; acetic acid / 40 h / Heating; Reflux

3.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 - 20 °C

3.2: 0 - 65 °C

4.1: triethylamine; tris-(o-tolyl)phosphine / palladium diacetate / N,N-dimethyl-formamide / 3 h / 100 °C

5.1: dmap; triethylamine / chloroform / 0 - 20 °C

6.1: potassium carbonate / acetonitrile / 8 h / 80 °C

7.1: hydrogen / palladium on activated charcoal / ethanol / 12 h / 20 °C / 760.05 Torr

8.1: hydrogenchloride / diethyl ether; dichloromethane

With hydrogenchloride; dmap; ammonium acetate; hydrogen; sodium hydride; potassium carbonate; acetic acid; triethylamine; tris-(o-tolyl)phosphine; palladium on activated charcoal; palladium diacetate; In diethyl ether; ethanol; dichloromethane; chloroform; N,N-dimethyl-formamide; acetonitrile;