ChemicalBook CAS DataBase List N-((N-Methyl-N-((2-isopropyl-4-thiazolyl)methyl)amino)carbonyl)-L-valine methyl ester

N-((N-Methyl-N-((2-isopropyl-4-thiazolyl)methyl)amino)carbonyl)-L-valine methyl ester synthesis

5synthesis methods

Product Name:N-((N-Methyl-N-((2-isopropyl-4-thiazolyl)methyl)amino)carbonyl)-L-valine methyl ester
CAS Number:154248-99-4
Molecular formula:C15H25N3O3S
Molecular Weight:327.44

126147-70-4
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2-Isopropyl-4-(methylaminomethyl)thiazole

154212-60-9
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$45.00/50mg

N-((N-Methyl-N-((2-isopropyl-4-thiazolyl)methyl)amino)carbonyl)-L-valine methyl ester

154248-99-4
33 suppliers
$85.00/2mg

Yield:154248-99-4 76.9%

Reaction Conditions:

with sodium hydroxide in n-heptane;water;ethyl acetate;toluene;

Steps:

27.C N-(N-Methyl-N-((2-isopropyl-4-thiazolyl)methyl)amino)carbonyl)-L-valine Methyl Ester

EXAMPLE 27C N-(N-Methyl-N-((2-isopropyl-4-thiazolyl)methyl)amino)carbonyl)-L-valine Methyl Ester Into a 500 ml 3-neck round bottom flask equipped with mechanical stirrer, nitrogen atmosphere, thermocouple, heating mantle and condensor was charged the product of Example 27B (28.1 g, 0.165 mols), phenoxycarbonyl-(L)-valine (41.5 g, 0.165 mol) and 155 ml toluene. This solution was warmed to reflux (110° C.) and stirred for three hours, then cooled to 20°+-5° C. and washed with 2*69 ml 10% citric acid followed by 1*69 ml water, 1*116 mls 4% sodium hydroxide, 1*58 ml 4% sodium hydroxide and finally 1*58 ml water. The organic product solution was then treated with 3 grams of activated carbon at reflux for 15 minutes, filtered through infusorial earth to remove carbon, and the carbon/infusorial earth cake was washed with 25 ml hot toluene. Next the solvent was removed to afford a brown oil which solidifed upon cooling. This brown solid was dissolved with warming in 31 ml EtOAc and 257 ml heptane at 60°+-5° C. This solution was slowly cooled to 25° C., stirred 12 hours, cooled further to 0° C., and stirred 3 hours. The crystals were collected by filtration and washed with 50 ml 1:9 EtOAc/Heptane. The solid was dried in a 50° C. vacuum oven for 12 hours to afford 41.5 grams of the desired product as a tan-colored solid (76.9%).

References:

US5484801,1996,A

154212-60-9
135 suppliers
$45.00/50mg