N-(1-methylethyl)-2-[3-[3-(methyloxy)phenyl]-1-oxo-7-[(1E/Z)-4-(1-piperidinyl)-1-buten-1-yl]pyrrolo[1,2-a]pyrazin-2(1H)-yl]acetamide

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Chemical Name:N-(1-methylethyl)-2-[3-[3-(methyloxy)phenyl]-1-oxo-7-[(1E/Z)-4-(1-piperidinyl)-1-buten-1-yl]pyrrolo[1,2-a]pyrazin-2(1H)-yl]acetamide
CAS No.:1192685-74-7
Molecular Formula:C₂₈H₃₆N₄O₃
Molecular Weight:476.619
Hs Code.:

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

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

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

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

: 110-89-4
piperidine

: 1192685-72-5
(3E/Z)-4-{2-{2-[(1-methylethyl)amino]-2-oxoethyl}-3-[3-(methyloxy)-phenyl]-1-oxo-1,2-dihydropyrrolo[1,2-a]pyrazin-7-yl}-3-buten-1-yl methanesulfonate

: 1192685-74-7
N-(1-methylethyl)-2-[3-[3-(methyloxy)phenyl]-1-oxo-7-[(1E/Z)-4-(1-piperidinyl)-1-buten-1-yl]pyrrolo[1,2-a]pyrazin-2(1H)-yl]acetamide

Guidance literature:: With potassium carbonate; In acetonitrile; at 80 ℃; for 8h;

Reference yield:

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

: 1192685-74-7
N-(1-methylethyl)-2-[3-[3-(methyloxy)phenyl]-1-oxo-7-[(1E/Z)-4-(1-piperidinyl)-1-buten-1-yl]pyrrolo[1,2-a]pyrazin-2(1H)-yl]acetamide

Guidance literature:: Multi-step reaction with 6 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

With dmap; ammonium acetate; sodium hydride; potassium carbonate; acetic acid; triethylamine; tris-(o-tolyl)phosphine; palladium diacetate; In chloroform; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 1192685-64-5
7-iodo-3-[3-(methyloxy)phenyl]-1H-pyrrolo[2,1-c][1,4]oxazin-1-one

: 1192685-74-7
N-(1-methylethyl)-2-[3-[3-(methyloxy)phenyl]-1-oxo-7-[(1E/Z)-4-(1-piperidinyl)-1-buten-1-yl]pyrrolo[1,2-a]pyrazin-2(1H)-yl]acetamide

Guidance literature:: Multi-step reaction with 5 steps

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

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

2.2: 0 - 65 °C

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

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

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

With dmap; ammonium acetate; sodium hydride; potassium carbonate; acetic acid; triethylamine; tris-(o-tolyl)phosphine; palladium diacetate; In chloroform; N,N-dimethyl-formamide; acetonitrile;