N-cyclopropyl-3-[3-{[(1R,2R)-3-hydroxy-2-methyl-1-phenylpropyl]amino}-2-oxopyrazin-1(2H)-yl]-4-methylbenzamide

Base Information

Chemical Name:N-cyclopropyl-3-[3-{[(1R,2R)-3-hydroxy-2-methyl-1-phenylpropyl]amino}-2-oxopyrazin-1(2H)-yl]-4-methylbenzamide
CAS No.:1095003-51-2
Molecular Formula:C₂₅H₂₈N₄O₃
Molecular Weight:432.522
Hs Code.:

Synonyms:N-cyclopropyl-3-[3-{[(1R,2R)-3-hydroxy-2-methyl-1-phenylpropyl]amino}-2-oxopyrazin-1(2H)-yl]-4-methylbenzamide

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Chemical Property of N-cyclopropyl-3-[3-{[(1R,2R)-3-hydroxy-2-methyl-1-phenylpropyl]amino}-2-oxopyrazin-1(2H)-yl]-4-methylbenzamide

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Technology Process of N-cyclopropyl-3-[3-{[(1R,2R)-3-hydroxy-2-methyl-1-phenylpropyl]amino}-2-oxopyrazin-1(2H)-yl]-4-methylbenzamide

There total 7 articles about N-cyclopropyl-3-[3-{[(1R,2R)-3-hydroxy-2-methyl-1-phenylpropyl]amino}-2-oxopyrazin-1(2H)-yl]-4-methylbenzamide 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:

: 1095005-58-5
methyl 3-[(cyanomethyl)amino]-4-methylbenzoate

: 1095003-51-2
N-cyclopropyl-3-[3-{[(1R,2R)-3-hydroxy-2-methyl-1-phenylpropyl]amino}-2-oxopyrazin-1(2H)-yl]-4-methylbenzamide

Guidance literature:: Multi-step reaction with 4 steps

1: 1,2-dichloro-benzene / 4 h / 100 °C

2: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 24 h / 50 °C

3: ammonium formate; N-ethyl-N,N-diisopropylamine / palladium 10% on activated carbon / ethanol / 2 h / 70 °C

4: isopropylmagnesium chloride / tetrahydrofuran / 0.25 h / 0 °C

With isopropylmagnesium chloride; ammonium formate; N-ethyl-N,N-diisopropylamine; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; 1,2-dichloro-benzene;

Reference yield:

: 1095005-59-6
methyl 3-(3,5-dibromo-2-oxopyrazin-1(2H)-yl)-4-methylbenzoate

: 1095003-51-2
N-cyclopropyl-3-[3-{[(1R,2R)-3-hydroxy-2-methyl-1-phenylpropyl]amino}-2-oxopyrazin-1(2H)-yl]-4-methylbenzamide

Guidance literature:: Multi-step reaction with 3 steps

1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 24 h / 50 °C

2: ammonium formate; N-ethyl-N,N-diisopropylamine / palladium 10% on activated carbon / ethanol / 2 h / 70 °C

3: isopropylmagnesium chloride / tetrahydrofuran / 0.25 h / 0 °C

With isopropylmagnesium chloride; ammonium formate; N-ethyl-N,N-diisopropylamine; palladium 10% on activated carbon; In tetrahydrofuran; ethanol;

Reference yield:

: 18595-18-1
3-amino-4-methyl benzoic acid methyl ester

: 1095003-51-2
N-cyclopropyl-3-[3-{[(1R,2R)-3-hydroxy-2-methyl-1-phenylpropyl]amino}-2-oxopyrazin-1(2H)-yl]-4-methylbenzamide

Guidance literature:: Multi-step reaction with 5 steps

1: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 12 h / Heating / reflux

2: 1,2-dichloro-benzene / 4 h / 100 °C

3: N-ethyl-N,N-diisopropylamine / tetrahydrofuran / 24 h / 50 °C

4: ammonium formate; N-ethyl-N,N-diisopropylamine / palladium 10% on activated carbon / ethanol / 2 h / 70 °C

5: isopropylmagnesium chloride / tetrahydrofuran / 0.25 h / 0 °C

With isopropylmagnesium chloride; ammonium formate; N-ethyl-N,N-diisopropylamine; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; 1,2-dichloro-benzene;