6-bromo-7-(3-fluorophenyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-8-carboxamide

Base Information

Chemical Name:6-bromo-7-(3-fluorophenyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-8-carboxamide
CAS No.:1352087-67-2
Molecular Formula:C₁₄H₁₃BrFN₃O
Molecular Weight:338.179
Hs Code.:

Synonyms:6-bromo-7-(3-fluorophenyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-8-carboxamide

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Chemical Property of 6-bromo-7-(3-fluorophenyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-8-carboxamide

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Technology Process of 6-bromo-7-(3-fluorophenyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-8-carboxamide

There total 12 articles about 6-bromo-7-(3-fluorophenyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-8-carboxamide 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:

: 1352087-66-1
tert-butyl 8-carbamoyl-6-bromo-7-(3-fluoro-phenyl)-3,4-dihydropyrrolo[1,2-a]pyrazine-2(1H)-carboxylate

: 1352087-67-2
6-bromo-7-(3-fluorophenyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-8-carboxamide

Guidance literature:: tert-butyl 8-carbamoyl-6-bromo-7-(3-fluoro-phenyl)-3,4-dihydropyrrolo[1,2-a]pyrazine-2(1H)-carboxylate; With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 1h;

With ammonium hydroxide; In water;

Reference yield:

: 1352087-60-5
ethyl 6-chloro-7-(3-fluorophenyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-8-carboxylate

: 1352087-67-2
6-bromo-7-(3-fluorophenyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-8-carboxamide

Guidance literature:: Multi-step reaction with 7 steps

1: dichloromethane / 0.5 h / 20 °C

2: ammonium formate / palladium 10% on activated carbon / methanol / 0.75 h / Reflux

3: N-Bromosuccinimide / tetrahydrofuran / 1.5 h / 20 °C

4: sodium hydroxide; water / ethanol / 48 h / 70 °C

5: tetrahydrofuran / 1 h / 50 °C

6: ammonium hydroxide / water / 5.5 h / 90 °C / autoclave

7: trifluoroacetic acid / dichloromethane / 1 h / 20 °C

With ammonium hydroxide; N-Bromosuccinimide; water; ammonium formate; trifluoroacetic acid; sodium hydroxide; palladium 10% on activated carbon; In tetrahydrofuran; methanol; ethanol; dichloromethane; water;

Reference yield:

: 1352087-61-6
2-tert-butyl 8-ethyl 6-chloro-7-(3-fluorophenyl)-3,4-dihydropyrrolo[1,2-a]pyrazine-2,8(1H)-dicarboxylate

: 1352087-67-2
6-bromo-7-(3-fluorophenyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-8-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1: ammonium formate / palladium 10% on activated carbon / methanol / 0.75 h / Reflux

2: N-Bromosuccinimide / tetrahydrofuran / 1.5 h / 20 °C

3: sodium hydroxide; water / ethanol / 48 h / 70 °C

4: tetrahydrofuran / 1 h / 50 °C

5: ammonium hydroxide / water / 5.5 h / 90 °C / autoclave

6: trifluoroacetic acid / dichloromethane / 1 h / 20 °C

With ammonium hydroxide; N-Bromosuccinimide; water; ammonium formate; trifluoroacetic acid; sodium hydroxide; palladium 10% on activated carbon; In tetrahydrofuran; methanol; ethanol; dichloromethane; water;