N-(4-fluorobenzyl)-2-hydroxy-7-methoxy-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide

Base Information

Chemical Name:N-(4-fluorobenzyl)-2-hydroxy-7-methoxy-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide
CAS No.:1383785-73-6
Molecular Formula:C₁₈H₁₅FN₂O₅
Molecular Weight:358.326
Hs Code.:

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

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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

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

There total 7 articles about N-(4-fluorobenzyl)-2-hydroxy-7-methoxy-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: 86.0%

: 1383786-69-3
N-(4-fluorobenzyl)-2-(benzyloxy)-7-methoxy-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide

: 1383785-73-6
N-(4-fluorobenzyl)-2-hydroxy-7-methoxy-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide

Guidance literature:: With 5%-palladium/activated carbon; hydrogen; In methanol; N,N-dimethyl-formamide; at 20 ℃; for 3h;
DOI:10.1021/jm500109z

Reference yield: 86.0%

: 1383785-73-6
N-(4-fluorobenzyl)-2-hydroxy-7-methoxy-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide

Guidance literature:

Reference yield:

: 1609575-79-2
C₁₃H₁₄O₇

: 1383785-73-6
N-(4-fluorobenzyl)-2-hydroxy-7-methoxy-1,3-dioxo-1,2,3,4-tetrahydroisoquinoline-4-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; diisopropylamine / ethyl acetate / 13 h / -20 - 20 °C

2: potassium hydroxide / methanol / 12 h / 20 °C

3: toluene / 15 h / Reflux; Dean-Stark

4: 5%-palladium/activated carbon; hydrogen / methanol; N,N-dimethyl-formamide / 3 h / 20 °C

With 5%-palladium/activated carbon; hydrogen; (benzotriazo-1-yloxy)tris(dimethylamino)phosphonium hexafluorophosphate; diisopropylamine; potassium hydroxide; In methanol; ethyl acetate; N,N-dimethyl-formamide; toluene;
DOI:10.1021/jm500109z