N-(5-(5-chloro-2-methoxyphenyl)-1-isopentyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

Base Information

Chemical Name:N-(5-(5-chloro-2-methoxyphenyl)-1-isopentyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide
CAS No.:1260162-67-1
Molecular Formula:C₂₂H₂₃ClN₆O₂
Molecular Weight:438.917
Hs Code.:

Synonyms:N-(5-(5-chloro-2-methoxyphenyl)-1-isopentyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

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Chemical Property of N-(5-(5-chloro-2-methoxyphenyl)-1-isopentyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

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Technology Process of N-(5-(5-chloro-2-methoxyphenyl)-1-isopentyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

There total 4 articles about N-(5-(5-chloro-2-methoxyphenyl)-1-isopentyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide 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: 12.3%

: 1260169-01-4
5-(5-chloro-2-methoxyphenyl)-1-isopentyl-1H-pyrazole-4-amine

: 25940-35-6
pyrazolo[1,5-a] pyrimidine-3-carboxylic acid

: 1260162-67-1
N-(5-(5-chloro-2-methoxyphenyl)-1-isopentyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; ((3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V); dmap; In N,N-dimethyl-formamide; at 20 ℃; for 12h;

Reference yield:

: 1240573-73-2
1-isopentyl-4-nitro-1H-pyrazole

: 1260162-67-1
N-(5-(5-chloro-2-methoxyphenyl)-1-isopentyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: potassium carbonate; Trimethylacetic acid / palladium diacetate; catacxium A / N,N-dimethyl acetamide / 12 h / 120 °C

2: ethanol; ammonium chloride / iron / water / 2 h / 75 °C

3: N-ethyl-N,N-diisopropylamine; ((3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) / dmap / N,N-dimethyl-formamide / 12 h / 20 °C

With ethanol; potassium carbonate; ammonium chloride; N-ethyl-N,N-diisopropylamine; ((3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V); Trimethylacetic acid; dmap; palladium diacetate; iron; catacxium A; In N,N-dimethyl acetamide; water; N,N-dimethyl-formamide;

Reference yield:

: 1260169-00-3
5-(5-chloro-2-methoxyphenyl)-1-isopentyl-4-nitro-1H-pyrazole

: 1260162-67-1
N-(5-(5-chloro-2-methoxyphenyl)-1-isopentyl-1H-pyrazol-4-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: ethanol; ammonium chloride / iron / water / 2 h / 75 °C

2: N-ethyl-N,N-diisopropylamine; ((3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V) / dmap / N,N-dimethyl-formamide / 12 h / 20 °C

With ethanol; ammonium chloride; N-ethyl-N,N-diisopropylamine; ((3H-[1,2,3]triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate(V); dmap; iron; In water; N,N-dimethyl-formamide;