1-(2-ethyl-1,2,3,4-tetrahydroisoquinolin-4-yl)-3-(2-phenyl-2,4,5,6-tetrahydrocyclopenta[c]pyrazol-3-yl)urea

Base Information

Chemical Name:1-(2-ethyl-1,2,3,4-tetrahydroisoquinolin-4-yl)-3-(2-phenyl-2,4,5,6-tetrahydrocyclopenta[c]pyrazol-3-yl)urea
CAS No.:1610343-34-4
Molecular Formula:C₂₄H₂₇N₅O
Molecular Weight:401.511
Hs Code.:

Synonyms:1-(2-ethyl-1,2,3,4-tetrahydroisoquinolin-4-yl)-3-(2-phenyl-2,4,5,6-tetrahydrocyclopenta[c]pyrazol-3-yl)urea

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Chemical Property of 1-(2-ethyl-1,2,3,4-tetrahydroisoquinolin-4-yl)-3-(2-phenyl-2,4,5,6-tetrahydrocyclopenta[c]pyrazol-3-yl)urea

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Technology Process of 1-(2-ethyl-1,2,3,4-tetrahydroisoquinolin-4-yl)-3-(2-phenyl-2,4,5,6-tetrahydrocyclopenta[c]pyrazol-3-yl)urea

There total 4 articles about 1-(2-ethyl-1,2,3,4-tetrahydroisoquinolin-4-yl)-3-(2-phenyl-2,4,5,6-tetrahydrocyclopenta[c]pyrazol-3-yl)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: 27.0%

: 1610346-34-3
1-(2-phenyl-2,4,5,6-tetrahydrocyclopenta[c]pyrazol-3-yl)-3-(1,2,3,4-tetrahydroisoquinolin-4-yl)urea hydrochloride

: 75-03-6
ethyl iodide

: 1610343-34-4
1-(2-ethyl-1,2,3,4-tetrahydroisoquinolin-4-yl)-3-(2-phenyl-2,4,5,6-tetrahydrocyclopenta[c]pyrazol-3-yl)urea

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

: 116140-19-3
1,2,3,4-tetrahydroisoquinoline-4-carboxylic acid

: 1610343-34-4
1-(2-ethyl-1,2,3,4-tetrahydroisoquinolin-4-yl)-3-(2-phenyl-2,4,5,6-tetrahydrocyclopenta[c]pyrazol-3-yl)urea

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / dichloromethane / 20 °C

2.1: triethylamine; diphenylphosphoranyl azide / toluene / 0.5 h / 80 °C

2.2: 80 °C

3.1: hydrogenchloride / dichloromethane; isopropyl alcohol / 72 h / 20 °C

4.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C

With hydrogenchloride; diphenylphosphoranyl azide; triethylamine; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol; toluene;

Reference yield:

: 936829-00-4
2-[(tert-butoxy)carbonyl]-1,2,3,4-tetrahydroisoquinoline-4-carboxylic acid

: 1610343-34-4
1-(2-ethyl-1,2,3,4-tetrahydroisoquinolin-4-yl)-3-(2-phenyl-2,4,5,6-tetrahydrocyclopenta[c]pyrazol-3-yl)urea

Guidance literature:: Multi-step reaction with 3 steps

1.1: triethylamine; diphenylphosphoranyl azide / toluene / 0.5 h / 80 °C

1.2: 80 °C

2.1: hydrogenchloride / dichloromethane; isopropyl alcohol / 72 h / 20 °C

3.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 20 °C

With hydrogenchloride; diphenylphosphoranyl azide; triethylamine; N-ethyl-N,N-diisopropylamine; In dichloromethane; N,N-dimethyl-formamide; isopropyl alcohol; toluene;