2-(1-(4-(trifluoromethoxy)phenylsulfonyl)piperidin-4-yloxy)isoindoline-1,3-dione

Base Information

• Chemical Name: 2-(1-(4-(trifluoromethoxy)phenylsulfonyl)piperidin-4-yloxy)isoindoline-1,3-dione
• CAS No.: 1092408-10-0
• Molecular Formula: C₂₀H₁₇F₃N₂O₆S
• Molecular Weight: 470.426
• Mol file: 1092408-10-0.mol

Synonyms:2-(1-(4-(trifluoromethoxy)phenylsulfonyl)piperidin-4-yloxy)isoindoline-1,3-dione

Chemical Property of 2-(1-(4-(trifluoromethoxy)phenylsulfonyl)piperidin-4-yloxy)isoindoline-1,3-dione

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-(1-(4-(trifluoromethoxy)phenylsulfonyl)piperidin-4-yloxy)isoindoline-1,3-dione

There total 8 articles about 2-(1-(4-(trifluoromethoxy)phenylsulfonyl)piperidin-4-yloxy)isoindoline-1,3-dione 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: 84.0%

2-(piperidin-4-yloxy)isoindoline-1,3-dione hydrochloride (143796-93-4) + 4-(trifluoro-methoxy)benzene-1-sulfonyl chloride (94108-56-2) → 2-(1-(4-(trifluoromethoxy)phenylsulfonyl)piperidin-4-yloxy)isoindoline-1,3-dione (1092408-10-0)

Guidance literature:

2-(piperidin-4-yloxy)isoindoline-1,3-dione hydrochloride; With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 80 ℃; for 0.5h;

4-(trifluoro-methoxy)benzene-1-sulfonyl chloride; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 0.666667h; Product distribution / selectivity;

Reference yield: 80.0%

N-hydroxyphthalimide (524-38-9) + 1-(4-(trifluoromethoxy)phenylsulfonyl)piperidin-4-ol (1092408-14-4) → 2-(1-(4-(trifluoromethoxy)phenylsulfonyl)piperidin-4-yloxy)isoindoline-1,3-dione (1092408-10-0)

Guidance literature:

With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; at 0 - 20 ℃;

Reference yield:

4-piperidone hydrochloride (41979-39-9) → 2-(1-(4-(trifluoromethoxy)phenylsulfonyl)piperidin-4-yloxy)isoindoline-1,3-dione (1092408-10-0)

Guidance literature:

Multi-step reaction with 3 steps

1.1: N-ethyl-N,N-diisopropylamine / water; N,N-dimethyl-formamide / 0.5 h / 80 °C

1.2: 0 - 20 °C

2.1: sodium tetrahydroborate / methanol / 0.75 h / 0 °C

3.1: triphenylphosphine; diethylazodicarboxylate / tetrahydrofuran; toluene / 48 h / 0 - 20 °C

With sodium tetrahydroborate; N-ethyl-N,N-diisopropylamine; triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; methanol; water; N,N-dimethyl-formamide; toluene;

upstream raw materials:

N-hydroxyphthalimide

1-(4-(trifluoromethoxy)phenylsulfonyl)piperidin-4-ol

2-(piperidin-4-yloxy)isoindoline-1,3-dione hydrochloride

4-(trifluoro-methoxy)benzene-1-sulfonyl chloride

Downstream raw materials:

O-(1-(4-(trifluoromethoxy)phenylsulfonyl)piperidin-4-yl)hydroxylamine

1-(1-(4-(trifluoromethoxy)phenylsulfonyl)piperidin-4-yloxy)-3-(3,3,3-trifluoropropyl)urea

N₁-cyclopropyl-N₂-(1-(4-(trifluoromethoxy)phenylsulfonyl)piperidin-4-yloxy)oxalamide

1-(3-fluorophenyl)-3-(1-(4-(trifluoromethoxy)phenylsulfonyl)piperidin-4-yloxy)urea