tert-butyl (E)-4-(6-((5-(3-methoxystyryl)thiazol-2-yl)amino)-2-methylpyrimidin-4-yl)piperazine-1-carboxylate

Base Information

Chemical Name:tert-butyl (E)-4-(6-((5-(3-methoxystyryl)thiazol-2-yl)amino)-2-methylpyrimidin-4-yl)piperazine-1-carboxylate
CAS No.:936845-97-5
Molecular Formula:C₂₆H₃₂N₆O₃S
Molecular Weight:508.644
Hs Code.:

Synonyms:tert-butyl (E)-4-(6-((5-(3-methoxystyryl)thiazol-2-yl)amino)-2-methylpyrimidin-4-yl)piperazine-1-carboxylate

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Chemical Property of tert-butyl (E)-4-(6-((5-(3-methoxystyryl)thiazol-2-yl)amino)-2-methylpyrimidin-4-yl)piperazine-1-carboxylate

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Technology Process of tert-butyl (E)-4-(6-((5-(3-methoxystyryl)thiazol-2-yl)amino)-2-methylpyrimidin-4-yl)piperazine-1-carboxylate

There total 8 articles about tert-butyl (E)-4-(6-((5-(3-methoxystyryl)thiazol-2-yl)amino)-2-methylpyrimidin-4-yl)piperazine-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: 80.0%

: tert-butyl 4-(6-((5-(3-methoxystyryl)thiazol-2-yl)amino)-2-methylpyrimidin-4-yl)piperazine-1-carboxylate

: 936845-97-5
tert-butyl (E)-4-(6-((5-(3-methoxystyryl)thiazol-2-yl)amino)-2-methylpyrimidin-4-yl)piperazine-1-carboxylate

Guidance literature:: With iodine; In chloroform; at 20 ℃;
DOI:10.1021/acs.jmedchem.0c00967

Reference yield: 52.0%

: 936845-85-1
4-[6-(5-formyl-thiazol-2-ylamino)-2-methyl-pyrimidin-4-yl]-piperazine-1-carboxylic acid tert-butyl ester

: 72311-12-7
(3-methoxybenzyl)triphenylphosphonium bromide

: 936845-97-5
tert-butyl (E)-4-(6-((5-(3-methoxystyryl)thiazol-2-yl)amino)-2-methylpyrimidin-4-yl)piperazine-1-carboxylate

Guidance literature:: (3-methoxybenzyl)triphenylphosphonium bromide; With n-butyllithium; In tetrahydrofuran; hexane; at 0 ℃; for 0.5h;

4-[6-(5-formyl-thiazol-2-ylamino)-2-methyl-pyrimidin-4-yl]-piperazine-1-carboxylic acid tert-butyl ester; In tetrahydrofuran; hexane; at 20 ℃; for 1h;

Reference yield:

: 5-(3-methoxystyryl)thiazol-2-amine

: 936845-97-5
tert-butyl (E)-4-(6-((5-(3-methoxystyryl)thiazol-2-yl)amino)-2-methylpyrimidin-4-yl)piperazine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: potassium tert-butylate / tetrahydrofuran / 0 - 20 °C / Cooling with ice

2: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 120 °C

3: iodine / chloroform / 20 °C

With potassium tert-butylate; iodine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; chloroform; N,N-dimethyl-formamide;
DOI:10.1021/acs.jmedchem.0c00967