N-(3-(4-(dimethylamino)cyclohexyl)-1-p-tolyl-1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

Base Information

Chemical Name:N-(3-(4-(dimethylamino)cyclohexyl)-1-p-tolyl-1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide
CAS No.:1401218-22-1
Molecular Formula:C₂₅H₂₉N₇O
Molecular Weight:443.552
Hs Code.:

Synonyms:N-(3-(4-(dimethylamino)cyclohexyl)-1-p-tolyl-1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

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Chemical Property of N-(3-(4-(dimethylamino)cyclohexyl)-1-p-tolyl-1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

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Technology Process of N-(3-(4-(dimethylamino)cyclohexyl)-1-p-tolyl-1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

There total 8 articles about N-(3-(4-(dimethylamino)cyclohexyl)-1-p-tolyl-1H-pyrazol-5-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:

: 1401218-18-5
N-(3-(4-oxocyclohexyl)-1-p-tolyl-1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

: 124-40-3
dimethyl amine

: 1401218-22-1
N-(3-(4-(dimethylamino)cyclohexyl)-1-p-tolyl-1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

Guidance literature:: N-(3-(4-oxocyclohexyl)-1-p-tolyl-1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide; dimethyl amine; With sodium tris(acetoxy)borohydride; acetic acid; In tetrahydrofuran; dichloromethane; at 0 ℃; for 1h;

With sodium hydrogencarbonate; In tetrahydrofuran; dichloromethane; at 20 ℃;

Reference yield:

: 17159-79-4
ethyl 4-oxocyclohexane-1-carboxylate

: 1401218-22-1
N-(3-(4-(dimethylamino)cyclohexyl)-1-p-tolyl-1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: toluene-4-sulfonic acid / toluene / 18 h / Reflux

2.1: n-butyllithium / tetrahydrofuran; hexanes / 1 h / -78 °C

2.2: 19.25 h / -78 - 20 °C

3.1: montmorillonite K-10 clay / isopropyl alcohol / 0.83 h / 55 °C

4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h / 20 °C

5.1: hydrogenchloride; water / tetrahydrofuran / 72 h / 20 °C

6.1: sodium tris(acetoxy)borohydride / acetic acid / dichloromethane; tetrahydrofuran / 1 h / 0 °C

6.2: 20 °C

With hydrogenchloride; n-butyllithium; water; sodium tris(acetoxy)borohydride; N-ethyl-N,N-diisopropylamine; toluene-4-sulfonic acid; acetic acid; In tetrahydrofuran; hexanes; dichloromethane; isopropyl alcohol; toluene;

Reference yield:

: 1489-97-0
ethyl 1,4-dioxaspiro[4.5]decane-8-carboxylate

: 1401218-22-1
N-(3-(4-(dimethylamino)cyclohexyl)-1-p-tolyl-1H-pyrazol-5-yl)pyrazolo[1,5-a]pyrimidine-3-carboxamide

Guidance literature:: Multi-step reaction with 5 steps

1.1: n-butyllithium / tetrahydrofuran; hexanes / 1 h / -78 °C

1.2: 19.25 h / -78 - 20 °C

2.1: montmorillonite K-10 clay / isopropyl alcohol / 0.83 h / 55 °C

3.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 18 h / 20 °C

4.1: hydrogenchloride; water / tetrahydrofuran / 72 h / 20 °C

5.1: sodium tris(acetoxy)borohydride / acetic acid / dichloromethane; tetrahydrofuran / 1 h / 0 °C

5.2: 20 °C

With hydrogenchloride; n-butyllithium; water; sodium tris(acetoxy)borohydride; N-ethyl-N,N-diisopropylamine; acetic acid; In tetrahydrofuran; hexanes; dichloromethane; isopropyl alcohol;