tert-butyl 4-(5-(pyrazolo[1,5-a]pyrimidine-3-carboxamido)-1-(p-tolyl)-1H-pyrazol-3-yl)piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-(5-(pyrazolo[1,5-a]pyrimidine-3-carboxamido)-1-(p-tolyl)-1H-pyrazol-3-yl)piperidine-1-carboxylate
CAS No.:1401222-25-0
Molecular Formula:C₂₇H₃₁N₇O₃
Molecular Weight:501.588
Hs Code.:

Synonyms:tert-butyl 4-(5-(pyrazolo[1,5-a]pyrimidine-3-carboxamido)-1-(p-tolyl)-1H-pyrazol-3-yl)piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-(5-(pyrazolo[1,5-a]pyrimidine-3-carboxamido)-1-(p-tolyl)-1H-pyrazol-3-yl)piperidine-1-carboxylate

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Technology Process of tert-butyl 4-(5-(pyrazolo[1,5-a]pyrimidine-3-carboxamido)-1-(p-tolyl)-1H-pyrazol-3-yl)piperidine-1-carboxylate

There total 5 articles about tert-butyl 4-(5-(pyrazolo[1,5-a]pyrimidine-3-carboxamido)-1-(p-tolyl)-1H-pyrazol-3-yl)piperidine-1-carboxylate 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:

: 937602-40-9
pyrazolo[1,5-a]pyrimidine-3-carbonyl chloride

: C₂₀H₂₈N₄O₂

: 1401222-25-0
tert-butyl 4-(5-(pyrazolo[1,5-a]pyrimidine-3-carboxamido)-1-(p-tolyl)-1H-pyrazol-3-yl)piperidine-1-carboxylate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 2h; Inert atmosphere;
DOI:10.1021/acsmedchemlett.5b00106

Reference yield:

: 660406-84-8
4-(2-cyanoacetyl)piperidine-1-carboxylic acid tert-butyl ester

: 1401222-25-0
tert-butyl 4-(5-(pyrazolo[1,5-a]pyrimidine-3-carboxamido)-1-(p-tolyl)-1H-pyrazol-3-yl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: montmorillonite K-10 clay / isopropyl alcohol / 48 h / Reflux; Inert atmosphere

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 20 °C / Inert atmosphere

With N-ethyl-N,N-diisopropylamine; In dichloromethane; isopropyl alcohol;
DOI:10.1021/acsmedchemlett.5b00106

Reference yield:

: 539-44-6
N-4-methylphenylhydrazine

: 1401222-25-0
tert-butyl 4-(5-(pyrazolo[1,5-a]pyrimidine-3-carboxamido)-1-(p-tolyl)-1H-pyrazol-3-yl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: montmorillonite K-10 clay / isopropyl alcohol / 48 h / Reflux; Inert atmosphere

2: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 20 °C / Inert atmosphere

With N-ethyl-N,N-diisopropylamine; In dichloromethane; isopropyl alcohol;
DOI:10.1021/acsmedchemlett.5b00106