N-(4-fluorobenzyl)-7-benzamido-2-(benzyloxy)-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide

Base Information

Chemical Name:N-(4-fluorobenzyl)-7-benzamido-2-(benzyloxy)-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide
CAS No.:1383786-47-7
Molecular Formula:C₃₁H₂₄FN₃O₅
Molecular Weight:537.547
Hs Code.:

Synonyms:N-(4-fluorobenzyl)-7-benzamido-2-(benzyloxy)-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide

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Chemical Property of N-(4-fluorobenzyl)-7-benzamido-2-(benzyloxy)-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide

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Technology Process of N-(4-fluorobenzyl)-7-benzamido-2-(benzyloxy)-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide

There total 7 articles about N-(4-fluorobenzyl)-7-benzamido-2-(benzyloxy)-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide 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: 54.0%

: 1383786-46-6
methyl 7-benzamido-2-(benzyloxy)-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxylate

: 140-75-0
para-fluorobenzylamine

: 1383786-47-7
N-(4-fluorobenzyl)-7-benzamido-2-(benzyloxy)-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide

Guidance literature:: In toluene; Reflux; Dean-Stark;
DOI:10.1021/jm500109z

Reference yield:

: 7304-32-7
2-fluoro-5-nitrobenzoic acid

: 1383786-47-7
N-(4-fluorobenzyl)-7-benzamido-2-(benzyloxy)-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: thionyl chloride / 24 h / 0 °C / Reflux

2.1: sodium hydride / tetrahydrofuran; mineral oil / 0.5 h / 20 °C / Inert atmosphere

2.2: 15 h / Inert atmosphere; Reflux

3.1: 5%-palladium/activated carbon; hydrogen / methanol / 12 h / 20 °C

4.1: dichloromethane / 20 °C

5.1: toluene / Reflux; Dean-Stark

6.1: potassium hydroxide / methanol / 20 °C

7.1: toluene / Reflux; Dean-Stark

With thionyl chloride; 5%-palladium/activated carbon; hydrogen; sodium hydride; potassium hydroxide; In tetrahydrofuran; methanol; dichloromethane; toluene; mineral oil;
DOI:10.1021/jm500109z

Reference yield:

: 2965-22-2
methyl 2-fluoro-5-nitro-benzoate

: 1383786-47-7
N-(4-fluorobenzyl)-7-benzamido-2-(benzyloxy)-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium hydride / tetrahydrofuran; mineral oil / 0.5 h / 20 °C / Inert atmosphere

1.2: 15 h / Inert atmosphere; Reflux

2.1: 5%-palladium/activated carbon; hydrogen / methanol / 12 h / 20 °C

3.1: dichloromethane / 20 °C

4.1: toluene / Reflux; Dean-Stark

5.1: potassium hydroxide / methanol / 20 °C

6.1: toluene / Reflux; Dean-Stark

With 5%-palladium/activated carbon; hydrogen; sodium hydride; potassium hydroxide; In tetrahydrofuran; methanol; dichloromethane; toluene; mineral oil;
DOI:10.1021/jm500109z