(1S,2R)-2-[(1S)-1-[(pyridin-2-yloxy)methyl]-1,2,3,4-tetrahydroisoquinoline-2-carbonyl]cyclohexane-1-carboxylic acid

Base Information

Chemical Name:(1S,2R)-2-[(1S)-1-[(pyridin-2-yloxy)methyl]-1,2,3,4-tetrahydroisoquinoline-2-carbonyl]cyclohexane-1-carboxylic acid
CAS No.:1607007-45-3
Molecular Formula:C₂₃H₂₆N₂O₄
Molecular Weight:394.47
Hs Code.:

Synonyms:(1S,2R)-2-[(1S)-1-[(pyridin-2-yloxy)methyl]-1,2,3,4-tetrahydroisoquinoline-2-carbonyl]cyclohexane-1-carboxylic acid

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Chemical Property of (1S,2R)-2-[(1S)-1-[(pyridin-2-yloxy)methyl]-1,2,3,4-tetrahydroisoquinoline-2-carbonyl]cyclohexane-1-carboxylic acid

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Technology Process of (1S,2R)-2-[(1S)-1-[(pyridin-2-yloxy)methyl]-1,2,3,4-tetrahydroisoquinoline-2-carbonyl]cyclohexane-1-carboxylic acid

There total 11 articles about (1S,2R)-2-[(1S)-1-[(pyridin-2-yloxy)methyl]-1,2,3,4-tetrahydroisoquinoline-2-carbonyl]cyclohexane-1-carboxylic acid 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: 97.0%

: 1607007-44-2
benzyl (1S,2R)-2-[(1S)-1-[(pyridin-2-yloxy)methyl]-1,2,3,4-tetrahydroisoquinoline-2-carbonyl]cyclohexane-1-carboxylate

: 1607007-45-3
(1S,2R)-2-[(1S)-1-[(pyridin-2-yloxy)methyl]-1,2,3,4-tetrahydroisoquinoline-2-carbonyl]cyclohexane-1-carboxylic acid

Guidance literature:: With 5%-palladium/activated carbon; hydrogen; In ethanol; for 48h;
DOI:10.1002/cmdc.201300525

Reference yield:

: 872986-64-6
(S)-(1,2,3,4-tetrahydroisoquinolin-1-yl)methanol

: 1607007-45-3
(1S,2R)-2-[(1S)-1-[(pyridin-2-yloxy)methyl]-1,2,3,4-tetrahydroisoquinoline-2-carbonyl]cyclohexane-1-carboxylic acid

Guidance literature:: Multi-step reaction with 4 steps

1.1: 1H-imidazole; triethylamine; thionyl chloride / dichloromethane / 1 h / 0 °C

1.2: 1.5 h / 0 °C

2.1: caesium carbonate / N,N-dimethyl-formamide / 4 h / 20 - 60 °C

3.1: thionyl chloride / dichloromethane / 16 h / 20 °C

3.2: 5 h / 20 °C

4.1: 5%-palladium/activated carbon; hydrogen / ethanol / 48 h

With 1H-imidazole; thionyl chloride; 5%-palladium/activated carbon; hydrogen; caesium carbonate; triethylamine; In ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/cmdc.201300525

Reference yield:

: 1607007-21-5
(S)-1,5,6,10b-tetrahydro-3H-oxazolo[4,3-a]isoquinolin-3-one

: 1607007-45-3
(1S,2R)-2-[(1S)-1-[(pyridin-2-yloxy)methyl]-1,2,3,4-tetrahydroisoquinoline-2-carbonyl]cyclohexane-1-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: sodium hydroxide / ethanol / 1 h / Reflux

2.1: 1H-imidazole; triethylamine; thionyl chloride / dichloromethane / 1 h / 0 °C

2.2: 1.5 h / 0 °C

3.1: caesium carbonate / N,N-dimethyl-formamide / 4 h / 20 - 60 °C

4.1: thionyl chloride / dichloromethane / 16 h / 20 °C

4.2: 5 h / 20 °C

5.1: 5%-palladium/activated carbon; hydrogen / ethanol / 48 h

With 1H-imidazole; thionyl chloride; 5%-palladium/activated carbon; hydrogen; caesium carbonate; triethylamine; sodium hydroxide; In ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1002/cmdc.201300525