(R)-2-phenyl-cyclopropanecarboxylic acid [1-(4-fluoro-3-morpholin-4-yl-phenyl)-2-hydroxy-ethyl]-amide

Base Information

Chemical Name:(R)-2-phenyl-cyclopropanecarboxylic acid [1-(4-fluoro-3-morpholin-4-yl-phenyl)-2-hydroxy-ethyl]-amide
CAS No.:701913-77-1
Molecular Formula:C₂₂H₂₅FN₂O₃
Molecular Weight:384.451
Hs Code.:

Synonyms:(R)-2-phenyl-cyclopropanecarboxylic acid [1-(4-fluoro-3-morpholin-4-yl-phenyl)-2-hydroxy-ethyl]-amide

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Chemical Property of (R)-2-phenyl-cyclopropanecarboxylic acid [1-(4-fluoro-3-morpholin-4-yl-phenyl)-2-hydroxy-ethyl]-amide

Chemical Property:

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Technology Process of (R)-2-phenyl-cyclopropanecarboxylic acid [1-(4-fluoro-3-morpholin-4-yl-phenyl)-2-hydroxy-ethyl]-amide

There total 5 articles about (R)-2-phenyl-cyclopropanecarboxylic acid [1-(4-fluoro-3-morpholin-4-yl-phenyl)-2-hydroxy-ethyl]-amide 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:

: (R)-2-Amino-2-(4-fluoro-3-morpholin-4-yl-phenyl)-ethanol

: 5685-38-1
2-phenyl-cyclopropanecarboxylic acid

: 701913-77-1
(R)-2-phenyl-cyclopropanecarboxylic acid [1-(4-fluoro-3-morpholin-4-yl-phenyl)-2-hydroxy-ethyl]-amide

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; at 20 ℃;

Reference yield:

: 701914-09-2
2-bromo-1-fluoro-4-vinyl-benzene

: 701913-77-1
(R)-2-phenyl-cyclopropanecarboxylic acid [1-(4-fluoro-3-morpholin-4-yl-phenyl)-2-hydroxy-ethyl]-amide

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium phosphate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,2-dimethoxyethane / 4 h / Heating / reflux

2.1: sodium hydroxide; potassium osmate dihydrate; tert-butylhypochlorite / propan-1-ol; water / 0.08 h

2.2: 0.5 h / 20 °C

3.1: trifluoroacetic acid / dichloromethane / 2 h

4.1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 20 °C

With dmap; sodium hydroxide; potassium phosphate; potassium osmate dihydrate; tert-butylhypochlorite; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In propan-1-ol; 1,2-dimethoxyethane; dichloromethane; water;

Reference yield:

: 77771-02-9
3-bromo-4-fluorobenzaldehyde

: 701913-77-1
(R)-2-phenyl-cyclopropanecarboxylic acid [1-(4-fluoro-3-morpholin-4-yl-phenyl)-2-hydroxy-ethyl]-amide

Guidance literature:: Multi-step reaction with 5 steps

1.1: n-butyllithium / tetrahydrofuran / 1 h / 0 - 20 °C

1.2: 1 h / 0 - 20 °C

2.1: potassium phosphate / tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / 1,2-dimethoxyethane / 4 h / Heating / reflux

3.1: sodium hydroxide; potassium osmate dihydrate; tert-butylhypochlorite / propan-1-ol; water / 0.08 h

3.2: 0.5 h / 20 °C

4.1: trifluoroacetic acid / dichloromethane / 2 h

5.1: dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 20 °C

With dmap; sodium hydroxide; potassium phosphate; n-butyllithium; potassium osmate dihydrate; tert-butylhypochlorite; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; trifluoroacetic acid; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; In tetrahydrofuran; propan-1-ol; 1,2-dimethoxyethane; dichloromethane; water;