4-((7S)-7-{[(2R)-2-(4-chlorophenyl)-2-hydroxyethyl]amino}-5,6,7,8-tetrahydro-2-naphthalenyl)-2-methoxybenzoic acid hydrochloride

Base Information

Chemical Name:4-((7S)-7-{[(2R)-2-(4-chlorophenyl)-2-hydroxyethyl]amino}-5,6,7,8-tetrahydro-2-naphthalenyl)-2-methoxybenzoic acid hydrochloride
CAS No.:603122-46-9
Molecular Formula:C₂₆H₂₆ClNO₄*ClH
Molecular Weight:488.411
Hs Code.:

Synonyms:4-((7S)-7-{[(2R)-2-(4-chlorophenyl)-2-hydroxyethyl]amino}-5,6,7,8-tetrahydro-2-naphthalenyl)-2-methoxybenzoic acid hydrochloride

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Chemical Property of 4-((7S)-7-{[(2R)-2-(4-chlorophenyl)-2-hydroxyethyl]amino}-5,6,7,8-tetrahydro-2-naphthalenyl)-2-methoxybenzoic acid hydrochloride

Chemical Property:

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Technology Process of 4-((7S)-7-{[(2R)-2-(4-chlorophenyl)-2-hydroxyethyl]amino}-5,6,7,8-tetrahydro-2-naphthalenyl)-2-methoxybenzoic acid hydrochloride

There total 14 articles about 4-((7S)-7-{[(2R)-2-(4-chlorophenyl)-2-hydroxyethyl]amino}-5,6,7,8-tetrahydro-2-naphthalenyl)-2-methoxybenzoic acid hydrochloride 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:

: 2788-86-5,53649-47-1,97466-49-4,21019-51-2
(R)-2-(4-chlorophenyl)oxirane

: 603122-46-9
4-((7S)-7-{[(2R)-2-(4-chlorophenyl)-2-hydroxyethyl]amino}-5,6,7,8-tetrahydro-2-naphthalenyl)-2-methoxybenzoic acid hydrochloride

Guidance literature:: Multi-step reaction with 6 steps

1: ethanol / 18 h / Reflux

2: tetrahydrofuran / 12 h / 20 °C

3: 2,6-dimethylpyridine / dichloromethane / -78 °C

4: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate / water / 20 - 80 °C / Inert atmosphere

5: methanol; sodium hydroxide; water / 20 °C

6: hydrogenchloride / 1,4-dioxane / 20 °C

With 2,6-dimethylpyridine; hydrogenchloride; methanol; sodium hydroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; water; sodium carbonate; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; 4: Suzuki coupling;
DOI:10.1021/jm800222k

Reference yield:

: 603122-49-2
C₃₁H₃₄ClNO₆

: 603122-46-9
4-((7S)-7-{[(2R)-2-(4-chlorophenyl)-2-hydroxyethyl]amino}-5,6,7,8-tetrahydro-2-naphthalenyl)-2-methoxybenzoic acid hydrochloride

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; at 20 ℃;
DOI:10.1021/jm800222k

Reference yield:

: 1073-67-2,24991-47-7
4-vinylbenzyl chloride

: 603122-46-9
4-((7S)-7-{[(2R)-2-(4-chlorophenyl)-2-hydroxyethyl]amino}-5,6,7,8-tetrahydro-2-naphthalenyl)-2-methoxybenzoic acid hydrochloride

Guidance literature:: Multi-step reaction with 8 steps

1: AD-mixβ; water / tert-butyl alcohol / 4 h / Cooling with ice

2: Trimethyl orthoacetate; chloro-trimethyl-silane / dichloromethane / 1 h / Cooling with ice

3: ethanol / 18 h / Reflux

4: tetrahydrofuran / 12 h / 20 °C

5: 2,6-dimethylpyridine / dichloromethane / -78 °C

6: tetrakis(triphenylphosphine) palladium⁽⁰⁾; sodium carbonate / water / 20 - 80 °C / Inert atmosphere

7: methanol; sodium hydroxide; water / 20 °C

8: hydrogenchloride / 1,4-dioxane / 20 °C

With 2,6-dimethylpyridine; hydrogenchloride; methanol; Trimethyl orthoacetate; sodium hydroxide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; chloro-trimethyl-silane; AD-mixβ; water; sodium carbonate; In tetrahydrofuran; 1,4-dioxane; ethanol; dichloromethane; water; tert-butyl alcohol; 6: Suzuki coupling;
DOI:10.1021/jm800222k