1-((3-tert-butyl-1-(3-chlorophenyl)-1H-pyrazol-5-yl)methyl)-3-(6-(pyrrolidin-1-yl)pyridin-3-yl)urea

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Chemical Name:1-((3-tert-butyl-1-(3-chlorophenyl)-1H-pyrazol-5-yl)methyl)-3-(6-(pyrrolidin-1-yl)pyridin-3-yl)urea
CAS No.:1419600-56-8
Molecular Formula:C₂₄H₂₉ClN₆O
Molecular Weight:452.987
Hs Code.:

Synonyms:1-((3-tert-butyl-1-(3-chlorophenyl)-1H-pyrazol-5-yl)methyl)-3-(6-(pyrrolidin-1-yl)pyridin-3-yl)urea

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Chemical Property of 1-((3-tert-butyl-1-(3-chlorophenyl)-1H-pyrazol-5-yl)methyl)-3-(6-(pyrrolidin-1-yl)pyridin-3-yl)urea

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Technology Process of 1-((3-tert-butyl-1-(3-chlorophenyl)-1H-pyrazol-5-yl)methyl)-3-(6-(pyrrolidin-1-yl)pyridin-3-yl)urea

There total 5 articles about 1-((3-tert-butyl-1-(3-chlorophenyl)-1H-pyrazol-5-yl)methyl)-3-(6-(pyrrolidin-1-yl)pyridin-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: 88.0%

: 1254713-63-7
(3-tert-butyl-1-(3-chlorophenyl)-1H-pyrazol-5-yl)methanamine

: 1419603-97-6
phenyl 6-(pyrrolidin-1-yl)pyridin-3-ylcarbamate

: 1419600-56-8
1-((3-tert-butyl-1-(3-chlorophenyl)-1H-pyrazol-5-yl)methyl)-3-(6-(pyrrolidin-1-yl)pyridin-3-yl)urea

Guidance literature:: With triethylamine; In dimethyl sulfoxide; at 23 ℃;

Reference yield:

: 5418-51-9
5-nitro-2-hydroxypyridine

: 1419600-56-8
1-((3-tert-butyl-1-(3-chlorophenyl)-1H-pyrazol-5-yl)methyl)-3-(6-(pyrrolidin-1-yl)pyridin-3-yl)urea

Guidance literature:: Multi-step reaction with 5 steps

1: trichlorophosphate; phosphorus pentachloride / 16 h / 60 °C

2: 18-crown-6 ether; potassium carbonate / acetonitrile / Reflux

3: palladium 10% on activated carbon; hydrogen / methanol / 1 h / 23 °C

4: pyridine / acetonitrile / 1 h / 23 °C

5: triethylamine / dimethyl sulfoxide / 23 °C

With pyridine; 18-crown-6 ether; phosphorus pentachloride; palladium 10% on activated carbon; hydrogen; potassium carbonate; triethylamine; trichlorophosphate; In methanol; dimethyl sulfoxide; acetonitrile;

Reference yield:

: 4548-45-2
2-chloro-5-nitropyridine

: 1419600-56-8
1-((3-tert-butyl-1-(3-chlorophenyl)-1H-pyrazol-5-yl)methyl)-3-(6-(pyrrolidin-1-yl)pyridin-3-yl)urea

Guidance literature:: Multi-step reaction with 4 steps

1: 18-crown-6 ether; potassium carbonate / acetonitrile / Reflux

2: palladium 10% on activated carbon; hydrogen / methanol / 1 h / 23 °C

3: pyridine / acetonitrile / 1 h / 23 °C

4: triethylamine / dimethyl sulfoxide / 23 °C

With pyridine; 18-crown-6 ether; palladium 10% on activated carbon; hydrogen; potassium carbonate; triethylamine; In methanol; dimethyl sulfoxide; acetonitrile;