Indolizine derivatives and application thereof in medicines
A compound, isomer mixture technology, used in the field of medicine
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Embodiment 1
[0183] (7'-Hydroxy-5'-oxo-1'-phenyl-5'H-spiro[cyclopentane-1,8'-indolezine]-6'-carbonyl)glycine ( 1 )
[0184]
[0185] first step
[0186] 5-(1,3-dioxolan-2-yl)-3-oxo-4-phenylpentanoic acid ethyl ester ( 1b )
[0187]
[0188] Ethyl 3-oxo-4-phenylbutyrate (1.03 g, prepared according to the method described in the literature [European Journal of Medicinal Chemistry, 2014, vol 84, 312-334]) was dissolved in anhydrous tetrahydrofuran (20 ml), and ice Cool in a water bath, slowly add 60% pure mineral oil and sodium hydride mixed solids (200 mg) in small portions under nitrogen flow, and stir for 0.5 hours; then add hexamethylphosphoramide (2.7 g) and 1.6M A solution of n-butyllithium in hexane (3.13 mL); then 2-bromomethyl-1,3-dioxolane (840 mg) was added. The reaction was stirred overnight at room temperature. The reaction solution was carefully poured into saturated ammonium chloride aqueous solution, and then extracted with ethyl acetate; the ethyl acetate layer was...
Embodiment 2
[0212] (1'-(4-fluorophenyl)-7'-hydroxy-5'-oxo-5'H-spiro[cyclopentane-1,8'-indolezine]-6'-carbonyl) Glycine ( 2 )
[0213]
[0214] first step
[0215] 5-(1,3-dioxolan-2-yl)-4-(4-fluorophenyl)-3-oxopentanoic acid ethyl ester ( 2b )
[0216]
[0217] compound 2b According to the first step of embodiment 1 1b The synthetic method preparation, wherein raw material 2a : Ethyl 4-(4-fluorophenyl)-3-oxobutanoate was prepared according to the method described in the literature [European Journal of Medicinal Chemistry, 2014, vol 84, 312-334]. LCMS ESI(+):311(M+1) + .
[0218] second step
[0219] 1-(3-(1,3-dioxolan-2-yl)-2-(4-fluorophenyl)propionyl)cyclopentane-1-carboxylic acid ethyl ester ( 2c )
[0220]
[0221] compound 2c According to the second step of Example 1 1c Synthetic method from the compound 2b preparation. LCMS ESI(+):365(M+1) + .
[0222] third step
[0223] 1-(3-(4-fluorophenyl)-1H-pyrrol 0-2-yl)cyclopentane-1-carboxylic acid ethyl ester ( 2d...
Embodiment 3
[0239] (1'-(4-fluorophenyl)-7'-hydroxy-5'-oxo-5'H-spiro[cyclopentane-1,8'-indolezine]-6'-carbonyl) Ethyl glycinate ( 3 )
[0240]
[0241] compound 2 (1 equivalent) was suspended in ethanol (5 volumes), and thionyl chloride (4 equivalents) was carefully added dropwise; then refluxed until the reaction was complete. Naturally cooled to room temperature and then cooled in an ice-water bath, the solid was collected by filtration and washed with cold ethanol to obtain the compound 3 . LCMS ESI(+):427(M+1) + .
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