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

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Chemical Name:tert-butyl 8-carbamoyl-6-bromo-7-(3-fluoro-phenyl)-3,4-dihydropyrrolo[1,2-a]pyrazine-2(1H)-carboxylate
CAS No.:1352087-66-1
Molecular Formula:C₁₉H₂₁BrFN₃O₃
Molecular Weight:438.296
Hs Code.:

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

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

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

There total 12 articles about tert-butyl 8-carbamoyl-6-bromo-7-(3-fluoro-phenyl)-3,4-dihydropyrrolo[1,2-a]pyrazine-2(1H)-carboxylate 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:

: 1352087-65-0
tert-butyl 6-bromo-7-(3-fluorophenyl)-8-(1H-imidazol-1-ylcarbonyl)-3,4-dihydropyrrolo[1,2-a]pyrazine-2(1H)-carboxylate

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

Guidance literature:: With ammonium hydroxide; In water; at 90 ℃; for 5.5h; autoclave;

Reference yield:

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

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

Guidance literature:: Multi-step reaction with 6 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

With ammonium hydroxide; N-Bromosuccinimide; water; ammonium formate; 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

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

Guidance literature:: Multi-step reaction with 5 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

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