N-[5-(tert-butyl)-3-isoxazolyl]-N'-[4-(5-[2-methyl-6-(4-methylpiperazino)-4-pyrimidinyl]amino-1H-3-pyrazolyl)benzyl]urea

Base Information

Chemical Name:N-[5-(tert-butyl)-3-isoxazolyl]-N'-[4-(5-[2-methyl-6-(4-methylpiperazino)-4-pyrimidinyl]amino-1H-3-pyrazolyl)benzyl]urea
CAS No.:1395051-77-0
Molecular Formula:C₂₈H₃₆N₁₀O₂
Molecular Weight:544.66
Hs Code.:

Synonyms:N-[5-(tert-butyl)-3-isoxazolyl]-N'-[4-(5-[2-methyl-6-(4-methylpiperazino)-4-pyrimidinyl]amino-1H-3-pyrazolyl)benzyl]urea

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Chemical Property of N-[5-(tert-butyl)-3-isoxazolyl]-N'-[4-(5-[2-methyl-6-(4-methylpiperazino)-4-pyrimidinyl]amino-1H-3-pyrazolyl)benzyl]urea

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Technology Process of N-[5-(tert-butyl)-3-isoxazolyl]-N'-[4-(5-[2-methyl-6-(4-methylpiperazino)-4-pyrimidinyl]amino-1H-3-pyrazolyl)benzyl]urea

There total 6 articles about N-[5-(tert-butyl)-3-isoxazolyl]-N'-[4-(5-[2-methyl-6-(4-methylpiperazino)-4-pyrimidinyl]amino-1H-3-pyrazolyl)benzyl]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:

: 1391621-82-1
C₂₀H₂₆N₈

: C₁₅H₁₇N₃O₅

: 1395051-77-0
N-[5-(tert-butyl)-3-isoxazolyl]-N'-[4-(5-[2-methyl-6-(4-methylpiperazino)-4-pyrimidinyl]amino-1H-3-pyrazolyl)benzyl]urea

Guidance literature:: With sodium hydrogencarbonate; In dimethyl sulfoxide; at 50 ℃;
DOI:10.1016/j.bmc.2013.03.083

Reference yield:

: 1780-26-3
2,4-dichloro-2-methylpyrimidine

: 1395051-77-0
N-[5-(tert-butyl)-3-isoxazolyl]-N'-[4-(5-[2-methyl-6-(4-methylpiperazino)-4-pyrimidinyl]amino-1H-3-pyrazolyl)benzyl]urea

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogenchloride / N,N-dimethyl-formamide; 1,4-dioxane / 4 h / 20 - 80 °C

2: pyridine / 2 h / 20 - 80 °C

3: hydrogen; palladium 10% on activated carbon; hydrogenchloride / methanol; water / 12 h / 20 °C

4: sodium hydrogencarbonate / dimethyl sulfoxide / 50 °C

With hydrogenchloride; palladium 10% on activated carbon; hydrogen; sodium hydrogencarbonate; In 1,4-dioxane; pyridine; methanol; water; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2013.03.083

Reference yield:

: 1391621-80-9
benzyl N-[4-(5-amino-1H-3-pyrazolyl)benzyl]carbamate

: 1395051-77-0
N-[5-(tert-butyl)-3-isoxazolyl]-N'-[4-(5-[2-methyl-6-(4-methylpiperazino)-4-pyrimidinyl]amino-1H-3-pyrazolyl)benzyl]urea

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogenchloride / N,N-dimethyl-formamide; 1,4-dioxane / 4 h / 20 - 80 °C

2: pyridine / 2 h / 20 - 80 °C

3: hydrogen; palladium 10% on activated carbon; hydrogenchloride / methanol; water / 12 h / 20 °C

4: sodium hydrogencarbonate / dimethyl sulfoxide / 50 °C

With hydrogenchloride; palladium 10% on activated carbon; hydrogen; sodium hydrogencarbonate; In 1,4-dioxane; pyridine; methanol; water; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2013.03.083