1-(2-(4-fluorophenoxy)ethyl)-3-(1-(3-(trifluoromethyl)phenylsulfonyl)piperidin-4-yloxy)urea

Base Information

Chemical Name:1-(2-(4-fluorophenoxy)ethyl)-3-(1-(3-(trifluoromethyl)phenylsulfonyl)piperidin-4-yloxy)urea
CAS No.:1200797-13-2
Molecular Formula:C₂₁H₂₃F₄N₃O₅S
Molecular Weight:505.49
Hs Code.:

Synonyms:1-(2-(4-fluorophenoxy)ethyl)-3-(1-(3-(trifluoromethyl)phenylsulfonyl)piperidin-4-yloxy)urea

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Chemical Property of 1-(2-(4-fluorophenoxy)ethyl)-3-(1-(3-(trifluoromethyl)phenylsulfonyl)piperidin-4-yloxy)urea

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Technology Process of 1-(2-(4-fluorophenoxy)ethyl)-3-(1-(3-(trifluoromethyl)phenylsulfonyl)piperidin-4-yloxy)urea

There total 11 articles about 1-(2-(4-fluorophenoxy)ethyl)-3-(1-(3-(trifluoromethyl)phenylsulfonyl)piperidin-4-yloxy)urea 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: 32.0%

: 6096-89-5
2-(4-fluorophenoxy)-1-ethylamine

: 1200797-99-4
O-(1-(3-(trifluoromethyl)phenylsulfonyl)piperidin-4-yl)hydroxylamine

: 530-62-1
1,1'-carbonyldiimidazole

: 1200797-13-2
1-(2-(4-fluorophenoxy)ethyl)-3-(1-(3-(trifluoromethyl)phenylsulfonyl)piperidin-4-yloxy)urea

Guidance literature:: O-(1-(3-(trifluoromethyl)phenylsulfonyl)piperidin-4-yl)hydroxylamine; 1,1'-carbonyldiimidazole; With triethylamine; In dichloromethane; at 20 ℃; for 24h;

2-(4-fluorophenoxy)-1-ethylamine; In dichloromethane; at 20 ℃; for 17h;

Reference yield:

: 109384-19-2
t-butyl 4-hydroxy piperidine-1-carboxylate

: 1200797-13-2
1-(2-(4-fluorophenoxy)ethyl)-3-(1-(3-(trifluoromethyl)phenylsulfonyl)piperidin-4-yloxy)urea

Guidance literature:: Multi-step reaction with 5 steps

1.1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran / 0 - 20 °C

2.1: 0.5 h / 20 °C

3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 17 h / 20 °C

4.1: hydrazine hydrate / ethanol / 0.5 h / 20 °C

5.1: triethylamine / dichloromethane / 24 h / 20 °C

5.2: 17 h / 20 °C

With hydrazine hydrate; triethylamine; N-ethyl-N,N-diisopropylamine; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; ethanol; dichloromethane; 1.1: Mitsunobu reaction;

Reference yield:

: 143539-99-5
tert-butyl 4-(1,3-dioxo-1,3-dihydroisoindol-2-yloxy)piperidine-1-carboxylate

: 1200797-13-2
1-(2-(4-fluorophenoxy)ethyl)-3-(1-(3-(trifluoromethyl)phenylsulfonyl)piperidin-4-yloxy)urea

Guidance literature:: Multi-step reaction with 4 steps

1.1: 0.5 h / 20 °C

2.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 17 h / 20 °C

3.1: hydrazine hydrate / ethanol / 0.5 h / 20 °C

4.1: triethylamine / dichloromethane / 24 h / 20 °C

4.2: 17 h / 20 °C

With hydrazine hydrate; triethylamine; N-ethyl-N,N-diisopropylamine; In ethanol; dichloromethane;