4-(6-(2-methoxyethoxy)-1,2,3,4-tetrahydroisoquinoline-1-carboxamido)benzoic acid trifluoroacetate

Base Information

Chemical Name:4-(6-(2-methoxyethoxy)-1,2,3,4-tetrahydroisoquinoline-1-carboxamido)benzoic acid trifluoroacetate
CAS No.:1430217-41-6
Molecular Formula:C₂HF₃O₂*C₂₀H₂₂N₂O₅
Molecular Weight:484.429
Hs Code.:

Synonyms:4-(6-(2-methoxyethoxy)-1,2,3,4-tetrahydroisoquinoline-1-carboxamido)benzoic acid trifluoroacetate

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Chemical Property of 4-(6-(2-methoxyethoxy)-1,2,3,4-tetrahydroisoquinoline-1-carboxamido)benzoic acid trifluoroacetate

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Technology Process of 4-(6-(2-methoxyethoxy)-1,2,3,4-tetrahydroisoquinoline-1-carboxamido)benzoic acid trifluoroacetate

There total 3 articles about 4-(6-(2-methoxyethoxy)-1,2,3,4-tetrahydroisoquinoline-1-carboxamido)benzoic acid trifluoroacetate 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:

: 350014-19-6
methyl N-(tert-butyloxycarbonyl)-6-hydroxy-3,4-dihydro-1H-isoquinoline-1-carboxylate

: 1430217-41-6
4-(6-(2-methoxyethoxy)-1,2,3,4-tetrahydroisoquinoline-1-carboxamido)benzoic acid trifluoroacetate

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / N,N-dimethyl-formamide / 80 °C

2: methanol; lithium hydroxide / tetrahydrofuran; water / 14 h

3: pyridine; trichlorophosphate / 2 h / -10 °C

4: dichloromethane / 2 h

With pyridine; methanol; potassium carbonate; lithium hydroxide; trichlorophosphate; In tetrahydrofuran; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: C₁₉H₂₇NO₆

: 1430217-41-6
4-(6-(2-methoxyethoxy)-1,2,3,4-tetrahydroisoquinoline-1-carboxamido)benzoic acid trifluoroacetate

Guidance literature:: Multi-step reaction with 3 steps

1: methanol; lithium hydroxide / tetrahydrofuran; water / 14 h

2: pyridine; trichlorophosphate / 2 h / -10 °C

3: dichloromethane / 2 h

With pyridine; methanol; lithium hydroxide; trichlorophosphate; In tetrahydrofuran; dichloromethane; water;

Reference yield:

: C₁₈H₂₅NO₆

: 1430217-41-6
4-(6-(2-methoxyethoxy)-1,2,3,4-tetrahydroisoquinoline-1-carboxamido)benzoic acid trifluoroacetate

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine; trichlorophosphate / 2 h / -10 °C

2: dichloromethane / 2 h

With pyridine; trichlorophosphate; In dichloromethane;