(3aS,6aS)-3-[4-(acetyloxy)phenyl]-5,6a-dihydro-1-phenyl-5-[(1R)-1-phenylethyl]pyrrolo[3,4-c]pyrazole-4,6(1H,3aH)dione

Base Information

• Chemical Name: (3aS,6aS)-3-[4-(acetyloxy)phenyl]-5,6a-dihydro-1-phenyl-5-[(1R)-1-phenylethyl]pyrrolo[3,4-c]pyrazole-4,6(1H,3aH)dione
• CAS No.: 1262109-78-3
• Molecular Formula: C₂₇H₂₃N₃O₄
• Molecular Weight: 453.497

Synonyms:(3aS,6aS)-3-[4-(acetyloxy)phenyl]-5,6a-dihydro-1-phenyl-5-[(1R)-1-phenylethyl]pyrrolo[3,4-c]pyrazole-4,6(1H,3aH)dione

Chemical Property of (3aS,6aS)-3-[4-(acetyloxy)phenyl]-5,6a-dihydro-1-phenyl-5-[(1R)-1-phenylethyl]pyrrolo[3,4-c]pyrazole-4,6(1H,3aH)dione

Chemical Property:

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Technology Process of (3aS,6aS)-3-[4-(acetyloxy)phenyl]-5,6a-dihydro-1-phenyl-5-[(1R)-1-phenylethyl]pyrrolo[3,4-c]pyrazole-4,6(1H,3aH)dione

There total 6 articles about (3aS,6aS)-3-[4-(acetyloxy)phenyl]-5,6a-dihydro-1-phenyl-5-[(1R)-1-phenylethyl]pyrrolo[3,4-c]pyrazole-4,6(1H,3aH)dione 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: 71.0%

(R)-1-(1-phenylethyl)-1H-pyrrole-2,5-dione (60925-76-0,89143-10-2,94132-27-1,6129-15-3) + 4-Acetoxybenzoylchloridphenylhydrazon (50656-02-5) → (3aS,6aS)-3-[4-(acetyloxy)phenyl]-5,6a-dihydro-1-phenyl-5-[(1R)-1-phenylethyl]pyrrolo[3,4-c]pyrazole-4,6(1H,3aH)dione (1262109-78-3)

Guidance literature:

With triethylamine; In toluene; at 20 ℃; for 3h; regioselective reaction;

DOI:10.1007/s00706-011-0618-z

Reference yield:

4-formylphenyl acetate (878-00-2) → (3aS,6aS)-3-[4-(acetyloxy)phenyl]-5,6a-dihydro-1-phenyl-5-[(1R)-1-phenylethyl]pyrrolo[3,4-c]pyrazole-4,6(1H,3aH)dione (1262109-78-3)

Guidance literature:

Multi-step reaction with 3 steps

1: ethanol; water / 1 h / 20 °C

2: N-chlorosuccinimide-dimethylsulfide complex / dichloromethane / -40 - 0 °C

3: triethylamine / toluene / 3 h / 20 °C

With N-chlorosuccinimide-dimethylsulfide complex; triethylamine; In ethanol; dichloromethane; water; toluene;

DOI:10.1007/s00706-011-0618-z

Reference yield:

C15H14N2O2 (101773-48-2) → (3aS,6aS)-3-[4-(acetyloxy)phenyl]-5,6a-dihydro-1-phenyl-5-[(1R)-1-phenylethyl]pyrrolo[3,4-c]pyrazole-4,6(1H,3aH)dione (1262109-78-3)

Guidance literature:

Multi-step reaction with 2 steps

1: N-chlorosuccinimide-dimethylsulfide complex / dichloromethane / -40 - 0 °C

2: triethylamine / toluene / 3 h / 20 °C

With N-chlorosuccinimide-dimethylsulfide complex; triethylamine; In dichloromethane; toluene;

DOI:10.1007/s00706-011-0618-z

upstream raw materials:

4-formylphenyl acetate

C₁₅H₁₄N₂O₂

(R)-1-phenyl-ethyl-amine

(R)-1-(1-phenylethyl)-1H-pyrrole-2,5-dione

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