8-(4-methoxybenzyl)-7-phenyl-3,5,6,8-tetrahydro-2H-pyrrolo[3,4-h]quinazolin-2-one

Base Information

• Chemical Name: 8-(4-methoxybenzyl)-7-phenyl-3,5,6,8-tetrahydro-2H-pyrrolo[3,4-h]quinazolin-2-one
• CAS No.: 1575821-67-8
• Molecular Formula: C₂₄H₂₁N₃O₂
• Molecular Weight: 383.45

Synonyms:8-(4-methoxybenzyl)-7-phenyl-3,5,6,8-tetrahydro-2H-pyrrolo[3,4-h]quinazolin-2-one

Chemical Property of 8-(4-methoxybenzyl)-7-phenyl-3,5,6,8-tetrahydro-2H-pyrrolo[3,4-h]quinazolin-2-one

Chemical Property:

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Technology Process of 8-(4-methoxybenzyl)-7-phenyl-3,5,6,8-tetrahydro-2H-pyrrolo[3,4-h]quinazolin-2-one

There total 4 articles about 8-(4-methoxybenzyl)-7-phenyl-3,5,6,8-tetrahydro-2H-pyrrolo[3,4-h]quinazolin-2-one 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: 60.0%

5-(hydroxymethylidene)-2-(4-methoxybenzyl)-1-phenyl-2,5,6,7-tetrahydro-4H-isoindol-4-one (1575822-11-5) + urea (57-13-6) → 8-(4-methoxybenzyl)-7-phenyl-3,5,6,8-tetrahydro-2H-pyrrolo[3,4-h]quinazolin-2-one (1575821-67-8)

Guidance literature:

In ethanol; for 24h; Inert atmosphere; Reflux;

DOI:10.1016/j.ejmech.2013.10.014

Reference yield:

4-oxo-1-phenyl-4,5,6,7-tetrahydroisoindole (202286-29-1) → 8-(4-methoxybenzyl)-7-phenyl-3,5,6,8-tetrahydro-2H-pyrrolo[3,4-h]quinazolin-2-one (1575821-67-8)

Guidance literature:

Multi-step reaction with 3 steps

1.1: sodium hydride / tetrahydrofuran; mineral oil / 1 h / 0 °C

1.2: 2 h / 0 - 20 °C

2.1: potassium tert-butylate / toluene / 3 h / 0 - 20 °C / Inert atmosphere

2.2: 24 h / 0 - 20 °C / Inert atmosphere

3.1: ethanol / 24 h / Inert atmosphere; Reflux

With potassium tert-butylate; sodium hydride; In tetrahydrofuran; ethanol; toluene; mineral oil;

DOI:10.1016/j.ejmech.2013.10.014

Reference yield:

p-methoxybenzyl chloride (824-94-2) → 8-(4-methoxybenzyl)-7-phenyl-3,5,6,8-tetrahydro-2H-pyrrolo[3,4-h]quinazolin-2-one (1575821-67-8)

Guidance literature:

Multi-step reaction with 3 steps

1.1: sodium hydride / tetrahydrofuran; mineral oil / 1 h / 0 °C

1.2: 2 h / 0 - 20 °C

2.1: potassium tert-butylate / toluene / 3 h / 0 - 20 °C / Inert atmosphere

2.2: 24 h / 0 - 20 °C / Inert atmosphere

3.1: ethanol / 24 h / Inert atmosphere; Reflux

With potassium tert-butylate; sodium hydride; In tetrahydrofuran; ethanol; toluene; mineral oil;

DOI:10.1016/j.ejmech.2013.10.014

upstream raw materials:

4-oxo-1-phenyl-4,5,6,7-tetrahydroisoindole

5-(hydroxymethylidene)-2-(4-methoxybenzyl)-1-phenyl-2,5,6,7-tetrahydro-4H-isoindol-4-one

urea

2-(4-methoxybenzyl)-1-phenyl-2,5,6,7-tetrahydro-4H-isoindol-4-one

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