(R)-1-(3-(ethylamino)-7-(trifluoromethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea

Base Information

Chemical Name:(R)-1-(3-(ethylamino)-7-(trifluoromethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea
CAS No.:1589537-41-6
Molecular Formula:C₁₈H₁₉F₃N₆O
Molecular Weight:392.384
Hs Code.:

Synonyms:(R)-1-(3-(ethylamino)-7-(trifluoromethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea

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Chemical Property of (R)-1-(3-(ethylamino)-7-(trifluoromethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea

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Technology Process of (R)-1-(3-(ethylamino)-7-(trifluoromethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea

There total 5 articles about (R)-1-(3-(ethylamino)-7-(trifluoromethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)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:

: 1589535-91-0
(R)-1-(3-(ethylamino)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea

: 2926-29-6
Langlois reagent

: 1589537-41-6
(R)-1-(3-(ethylamino)-7-(trifluoromethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea

Guidance literature:: With tert.-butylhydroperoxide; In water; dimethyl sulfoxide; 1,2-dichloro-ethane; for 36h;

Reference yield:

: 6-chloro-3-iodo-1-trityl-1H-pyrazolo[4,3-c]pyridine

: 1589537-41-6
(R)-1-(3-(ethylamino)-7-(trifluoromethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea

Guidance literature:: Multi-step reaction with 4 steps

1: rac-Pro-OH; copper(l) iodide; potassium carbonate / dimethyl sulfoxide / 24 h / 70 °C

2: chloro[2-(dicyclohexylphosphino)-3,6-dimethoxy-2’,4’,6’-triisopropyl-1,1’-biphenyl] [2-(2-aminoethyl)phenyl]palladium(II); sodium t-butanolate / tetrahydrofuran / 6 h / 20 - 50 °C / Inert atmosphere

3: triethylsilane; trifluoroacetic acid / 0.5 h / 20 °C

4: tert.-butylhydroperoxide / dimethyl sulfoxide; 1,2-dichloro-ethane; water / 36 h

With triethylsilane; tert.-butylhydroperoxide; copper(l) iodide; chloro[2-(dicyclohexylphosphino)-3,6-dimethoxy-2’,4’,6’-triisopropyl-1,1’-biphenyl] [2-(2-aminoethyl)phenyl]palladium(II); potassium carbonate; trifluoroacetic acid; rac-Pro-OH; sodium t-butanolate; In tetrahydrofuran; water; dimethyl sulfoxide; 1,2-dichloro-ethane;

Reference yield:

: 1589540-86-2
6-chloro-N-ethyl-1-trityl-1H-pyrazolo[4,3-c]pyridin-3-amine

: 1589537-41-6
(R)-1-(3-(ethylamino)-7-(trifluoromethyl)-1H-pyrazolo[4,3-c]pyridin-6-yl)-3-(1-phenylethyl)urea

Guidance literature:: Multi-step reaction with 3 steps

1: chloro[2-(dicyclohexylphosphino)-3,6-dimethoxy-2’,4’,6’-triisopropyl-1,1’-biphenyl] [2-(2-aminoethyl)phenyl]palladium(II); sodium t-butanolate / tetrahydrofuran / 6 h / 20 - 50 °C / Inert atmosphere

2: triethylsilane; trifluoroacetic acid / 0.5 h / 20 °C

3: tert.-butylhydroperoxide / dimethyl sulfoxide; 1,2-dichloro-ethane; water / 36 h

With triethylsilane; tert.-butylhydroperoxide; chloro[2-(dicyclohexylphosphino)-3,6-dimethoxy-2’,4’,6’-triisopropyl-1,1’-biphenyl] [2-(2-aminoethyl)phenyl]palladium(II); trifluoroacetic acid; sodium t-butanolate; In tetrahydrofuran; water; dimethyl sulfoxide; 1,2-dichloro-ethane;