(2-phenyl-7-p-tolylpyrazolo[1,5-a]pyrimidin-5-yl)(4-(2-(3,4,5-trimethoxybenzylamino)benzoyl)piperazin-1-yl)methanone

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Chemical Name:(2-phenyl-7-p-tolylpyrazolo[1,5-a]pyrimidin-5-yl)(4-(2-(3,4,5-trimethoxybenzylamino)benzoyl)piperazin-1-yl)methanone
CAS No.:1397211-81-2
Molecular Formula:C₄₁H₄₀N₆O₅
Molecular Weight:696.806
Hs Code.:

Synonyms:(2-phenyl-7-p-tolylpyrazolo[1,5-a]pyrimidin-5-yl)(4-(2-(3,4,5-trimethoxybenzylamino)benzoyl)piperazin-1-yl)methanone

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Chemical Property of (2-phenyl-7-p-tolylpyrazolo[1,5-a]pyrimidin-5-yl)(4-(2-(3,4,5-trimethoxybenzylamino)benzoyl)piperazin-1-yl)methanone

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Technology Process of (2-phenyl-7-p-tolylpyrazolo[1,5-a]pyrimidin-5-yl)(4-(2-(3,4,5-trimethoxybenzylamino)benzoyl)piperazin-1-yl)methanone

There total 7 articles about (2-phenyl-7-p-tolylpyrazolo[1,5-a]pyrimidin-5-yl)(4-(2-(3,4,5-trimethoxybenzylamino)benzoyl)piperazin-1-yl)methanone 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: 75.0%

: 1235987-71-9
piperazin-1-yl-(2-(3,4,5-trimethoxybenzylamino)phenyl)methanone

: 1397213-11-4
2-phenyl-7-p-tolylpyrazolo[1,5-a]pyrimidine-5-carboxylic acid

: 1397211-81-2
(2-phenyl-7-p-tolylpyrazolo[1,5-a]pyrimidin-5-yl)(4-(2-(3,4,5-trimethoxybenzylamino)benzoyl)piperazin-1-yl)methanone

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃; for 10h;
DOI:10.1002/cmdc.201200205

Reference yield:

: 1235987-65-1
C₂₆H₃₅N₃O₆

: 1397211-81-2
(2-phenyl-7-p-tolylpyrazolo[1,5-a]pyrimidin-5-yl)(4-(2-(3,4,5-trimethoxybenzylamino)benzoyl)piperazin-1-yl)methanone

Guidance literature:: Multi-step reaction with 2 steps

1: trifluoroacetic acid / dichloromethane / 5 h / 20 °C

2: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 10 h / 20 °C

With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; In dichloromethane;
DOI:10.1002/cmdc.201200205

Reference yield:

: 118-48-9
isatoic anhydride

: 1397211-81-2
(2-phenyl-7-p-tolylpyrazolo[1,5-a]pyrimidin-5-yl)(4-(2-(3,4,5-trimethoxybenzylamino)benzoyl)piperazin-1-yl)methanone

Guidance literature:: Multi-step reaction with 4 steps

1: 1,4-dioxane / 4 h / Reflux

2: sodium cyanoborohydride; acetic acid / methanol / 22 h / 20 °C

3: trifluoroacetic acid / dichloromethane / 5 h / 20 °C

4: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / dichloromethane / 10 h / 20 °C

With sodium cyanoborohydride; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; trifluoroacetic acid; In 1,4-dioxane; methanol; dichloromethane;
DOI:10.1002/cmdc.201200205