N-cyclopropyl-3-[2-(4-methoxybenzyl)-1-oxo-1,2-dihydroisoquinolin-6-yl]-4-methylbenzamide

Base Information

Chemical Name:N-cyclopropyl-3-[2-(4-methoxybenzyl)-1-oxo-1,2-dihydroisoquinolin-6-yl]-4-methylbenzamide
CAS No.:1070292-81-7
Molecular Formula:C₂₈H₂₆N₂O₃
Molecular Weight:438.526
Hs Code.:

Synonyms:N-cyclopropyl-3-[2-(4-methoxybenzyl)-1-oxo-1,2-dihydroisoquinolin-6-yl]-4-methylbenzamide

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Chemical Property of N-cyclopropyl-3-[2-(4-methoxybenzyl)-1-oxo-1,2-dihydroisoquinolin-6-yl]-4-methylbenzamide

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Technology Process of N-cyclopropyl-3-[2-(4-methoxybenzyl)-1-oxo-1,2-dihydroisoquinolin-6-yl]-4-methylbenzamide

There total 7 articles about N-cyclopropyl-3-[2-(4-methoxybenzyl)-1-oxo-1,2-dihydroisoquinolin-6-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:

: 1070292-87-3
3-[2-(4-methoxybenzyl)-1-oxo-1,2-dihydroisoquinolin-6-yl]-4-methylbenzoic acid methyl ester

: 765-30-0
Cyclopropylamine

: 1070292-81-7
N-cyclopropyl-3-[2-(4-methoxybenzyl)-1-oxo-1,2-dihydroisoquinolin-6-yl]-4-methylbenzamide

Guidance literature:: 3-[2-(4-methoxybenzyl)-1-oxo-1,2-dihydroisoquinolin-6-yl]-4-methylbenzoic acid methyl ester; Cyclopropylamine; With isopropylmagnesium chloride; In tetrahydrofuran; at 20 ℃; for 1h;

With water; ammonium chloride; In tetrahydrofuran;

Reference yield:

: 1070292-84-0
6-bromo-2-(4-methoxybenzyl)-4H-isoquinoline-1,3-dione

: 1070292-81-7
N-cyclopropyl-3-[2-(4-methoxybenzyl)-1-oxo-1,2-dihydroisoquinolin-6-yl]-4-methylbenzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium tetrahydroborate / methanol; dichloromethane / 2 h

1.2: 0.5 h

2.1: potassium carbonate / N,N-dimethyl-formamide / 17 h / 95 °C

3.1: isopropylmagnesium chloride / tetrahydrofuran / 1 h / 20 °C

With sodium tetrahydroborate; isopropylmagnesium chloride; potassium carbonate; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 943749-63-1
4-bromo-2-(carboxymethyl)benzoic acid

: 1070292-81-7
N-cyclopropyl-3-[2-(4-methoxybenzyl)-1-oxo-1,2-dihydroisoquinolin-6-yl]-4-methylbenzamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: acetyl chloride / acetone / 17 h / 20 °C

2.1: acetic acid / toluene / 17 h / Heating / reflux

3.1: sodium tetrahydroborate / methanol; dichloromethane / 2 h

3.2: 0.5 h

4.1: potassium carbonate / N,N-dimethyl-formamide / 17 h / 95 °C

5.1: isopropylmagnesium chloride / tetrahydrofuran / 1 h / 20 °C

With sodium tetrahydroborate; isopropylmagnesium chloride; potassium carbonate; acetic acid; acetyl chloride; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; acetone; toluene;