2,2-dichloro-N-{(1S,2R)-2-[4-(6-ethylaminomethylpyridin-3-yl)phenyl]-1-fluoromethyl-2-hydroxyethyl}acetamide

Base Information

Chemical Name:2,2-dichloro-N-{(1S,2R)-2-[4-(6-ethylaminomethylpyridin-3-yl)phenyl]-1-fluoromethyl-2-hydroxyethyl}acetamide
CAS No.:1454904-74-5
Molecular Formula:C₁₉H₂₂Cl₂FN₃O₂
Molecular Weight:414.307
Hs Code.:

Synonyms:2,2-dichloro-N-{(1S,2R)-2-[4-(6-ethylaminomethylpyridin-3-yl)phenyl]-1-fluoromethyl-2-hydroxyethyl}acetamide

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Chemical Property of 2,2-dichloro-N-{(1S,2R)-2-[4-(6-ethylaminomethylpyridin-3-yl)phenyl]-1-fluoromethyl-2-hydroxyethyl}acetamide

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Technology Process of 2,2-dichloro-N-{(1S,2R)-2-[4-(6-ethylaminomethylpyridin-3-yl)phenyl]-1-fluoromethyl-2-hydroxyethyl}acetamide

There total 8 articles about 2,2-dichloro-N-{(1S,2R)-2-[4-(6-ethylaminomethylpyridin-3-yl)phenyl]-1-fluoromethyl-2-hydroxyethyl}acetamide 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:

: (1R,2S)-2-amino-1-[4-(6-ethylaminomethylpyridin-3-yl)phenyl]-3-fluoropropan-1-ol

: 535-15-9
ethyl 1,1-dichloroacetate

: 1454904-74-5
2,2-dichloro-N-{(1S,2R)-2-[4-(6-ethylaminomethylpyridin-3-yl)phenyl]-1-fluoromethyl-2-hydroxyethyl}acetamide

Guidance literature:: With triethylamine; In methanol; at 20 ℃; for 16h;

Reference yield:

: 1454907-45-9
(4S,5R)-5-[4-(6-cyanopyridin-3-yl)phenyl]-4-fluoromethyl-2,2-dimethyloxazolidine-3-carboxylic acid tert-butyl ester

: 1454904-74-5
2,2-dichloro-N-{(1S,2R)-2-[4-(6-ethylaminomethylpyridin-3-yl)phenyl]-1-fluoromethyl-2-hydroxyethyl}acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: potassium hydroxide; methanol / 48 h / 65 °C

2: diisopropylamine; triphenylphosphine / tetrahydrofuran; ethyl acetate / 14 h / 20 °C

3: dimethylsulfide borane complex / tetrahydrofuran; toluene / 16 h / 0 - 65 °C

4: trifluoroacetic acid / dichloromethane / 2 h / 0 - 20 °C

5: triethylamine / methanol / 16 h / 20 °C

With methanol; dimethylsulfide borane complex; triethylamine; diisopropylamine; triphenylphosphine; trifluoroacetic acid; potassium hydroxide; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate; toluene;

Reference yield:

: 1454907-46-0
5-[4-((4S,5R)-3-tert-butoxycarbonyl-4-fluoromethyl-2,2-dimethyloxazolidin-5-yl)phenyl]pyridine-2-carboxylic acid

: 1454904-74-5
2,2-dichloro-N-{(1S,2R)-2-[4-(6-ethylaminomethylpyridin-3-yl)phenyl]-1-fluoromethyl-2-hydroxyethyl}acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: diisopropylamine; triphenylphosphine / tetrahydrofuran; ethyl acetate / 14 h / 20 °C

2: dimethylsulfide borane complex / tetrahydrofuran; toluene / 16 h / 0 - 65 °C

3: trifluoroacetic acid / dichloromethane / 2 h / 0 - 20 °C

4: triethylamine / methanol / 16 h / 20 °C

With dimethylsulfide borane complex; triethylamine; diisopropylamine; triphenylphosphine; trifluoroacetic acid; In tetrahydrofuran; methanol; dichloromethane; ethyl acetate; toluene;