1-({4-[5-(methylamino)-3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}methyl)-2-pyrrolidinone

Base Information

Chemical Name:1-({4-[5-(methylamino)-3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}methyl)-2-pyrrolidinone
CAS No.:1092459-37-4
Molecular Formula:C₂₀H₂₃F₃N₄O
Molecular Weight:392.424
Hs Code.:

Synonyms:1-({4-[5-(methylamino)-3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}methyl)-2-pyrrolidinone

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Chemical Property of 1-({4-[5-(methylamino)-3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}methyl)-2-pyrrolidinone

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Technology Process of 1-({4-[5-(methylamino)-3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}methyl)-2-pyrrolidinone

There total 4 articles about 1-({4-[5-(methylamino)-3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}methyl)-2-pyrrolidinone 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: 35.0%

: 950785-27-0
1-[(4-iodophenyl)methyl]-2-pyrrolidinone

: 1092459-58-9
N-methyl-3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-5-amine

: 1092459-37-4
1-({4-[5-(methylamino)-3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}methyl)-2-pyrrolidinone

Guidance literature:: With potassium carbonate; copper(I) oxide; dimethylaminoacetic acid; In dimethyl sulfoxide; at 190 ℃; for 0.5h; Microwave irradiation;

Reference yield:

: 16004-15-2
1-bromomethyl-4-iodobenzene

: 1092459-37-4
1-({4-[5-(methylamino)-3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}methyl)-2-pyrrolidinone

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydride / N,N-dimethyl-formamide / 0.67 h / Cooling with methanol-dry ice

1.2: 3 h / 20 °C

2.1: potassium carbonate / copper(I) oxide; dimethylaminoacetic acid / dimethyl sulfoxide / 0.5 h / 190 °C / Microwave irradiation

With sodium hydride; potassium carbonate; copper(I) oxide; dimethylaminoacetic acid; In dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

: 1092459-56-7
N-tert-butoxycarbonyl-4-oxo-3-(trifluoroacetyl)cyclohexylamine

: 1092459-37-4
1-({4-[5-(methylamino)-3-(trifluoromethyl)-4,5,6,7-tetrahydro-1H-indazol-1-yl]phenyl}methyl)-2-pyrrolidinone

Guidance literature:: Multi-step reaction with 3 steps

1: hydrazine / ethanol / 1.5 h / 50 - 60 °C

2: lithium aluminium tetrahydride / tetrahydrofuran / 4.5 h / 20 - 60 °C

3: potassium carbonate / copper(I) oxide; dimethylaminoacetic acid / dimethyl sulfoxide / 0.5 h / 190 °C / Microwave irradiation

With lithium aluminium tetrahydride; potassium carbonate; hydrazine; copper(I) oxide; dimethylaminoacetic acid; In tetrahydrofuran; ethanol; dimethyl sulfoxide;