N-{(1S)-2-[4-(6-ethoxy-2H-indazol-2-yl)-3-fluorophenoxy]-1-methylethyl}acetamide

Base Information

Chemical Name:N-{(1S)-2-[4-(6-ethoxy-2H-indazol-2-yl)-3-fluorophenoxy]-1-methylethyl}acetamide
CAS No.:1380066-94-3
Molecular Formula:C₂₀H₂₂FN₃O₃
Molecular Weight:371.411
Hs Code.:

Synonyms:N-{(1S)-2-[4-(6-ethoxy-2H-indazol-2-yl)-3-fluorophenoxy]-1-methylethyl}acetamide

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Chemical Property of N-{(1S)-2-[4-(6-ethoxy-2H-indazol-2-yl)-3-fluorophenoxy]-1-methylethyl}acetamide

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Technology Process of N-{(1S)-2-[4-(6-ethoxy-2H-indazol-2-yl)-3-fluorophenoxy]-1-methylethyl}acetamide

There total 6 articles about N-{(1S)-2-[4-(6-ethoxy-2H-indazol-2-yl)-3-fluorophenoxy]-1-methylethyl}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:

: 1380068-81-4
tert-butyl {(1S)-2-[4-(6-ethoxy-2H-indazol-2-yl)-3-fluorophenoxy]-1-methylethyl}carbamate

: 108-24-7
acetic anhydride

: 1380066-94-3
N-{(1S)-2-[4-(6-ethoxy-2H-indazol-2-yl)-3-fluorophenoxy]-1-methylethyl}acetamide

Guidance literature:: tert-butyl {(1S)-2-[4-(6-ethoxy-2H-indazol-2-yl)-3-fluorophenoxy]-1-methylethyl}carbamate; With hydrogenchloride; In ethyl acetate; at 20 ℃; for 1h;

acetic anhydride; With pyridine; at 20 ℃; for 1h;

Reference yield:

: 394-41-2
3-fluoro-4-nitrophenol

: 1380066-94-3
N-{(1S)-2-[4-(6-ethoxy-2H-indazol-2-yl)-3-fluorophenoxy]-1-methylethyl}acetamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: triphenylphosphine; di-isopropyl azodicarboxylate / toluene; tetrahydrofuran / 20 °C

2.1: hydrogen / palladium 10% on activated carbon / ethanol; water / 1 h / 20 °C

3.1: magnesium sulfate / ethanol / Reflux

3.2: 3 h / 130 °C

4.1: hydrogenchloride / ethyl acetate / 1 h / 20 °C

4.2: 1 h / 20 °C

With hydrogenchloride; di-isopropyl azodicarboxylate; hydrogen; magnesium sulfate; triphenylphosphine; palladium 10% on activated carbon; In tetrahydrofuran; ethanol; water; ethyl acetate; toluene;

Reference yield:

: 1380068-79-0
tert-butyl [(1S)-2-(3-fluoro-4-nitrophenoxy)-1-methylethyl]carbamate

: 1380066-94-3
N-{(1S)-2-[4-(6-ethoxy-2H-indazol-2-yl)-3-fluorophenoxy]-1-methylethyl}acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: hydrogen / palladium 10% on activated carbon / ethanol; water / 1 h / 20 °C

2.1: magnesium sulfate / ethanol / Reflux

2.2: 3 h / 130 °C

3.1: hydrogenchloride / ethyl acetate / 1 h / 20 °C

3.2: 1 h / 20 °C

With hydrogenchloride; hydrogen; magnesium sulfate; palladium 10% on activated carbon; In ethanol; water; ethyl acetate;