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HRID 448781作成日:2026年10月26日

L-Methioninol → N-[[1-[[[4-[2-(4-Methyl-1-piperazinyl)-4-thiazolyl]phenyl]carbonyl]amino]cyclohexyl]carbonyl]-L-methioninol

https://huagongshe.com/reaction/448781

反応式

関与物質

役割名称HCID仕込み量
反応物L-MethioninolHCID 2724404—
反応物2-[4-[2-(4-Methyl-1-piperazinyl)-4-thiazolyl]phenyl]-3-oxa-1-azaspiro[4.5]dec-1-en-4-oneHCID 57672803—
溶媒DimethylformamideHCID 6228—
生成物N-[[1-[[[4-[2-(4-Methyl-1-piperazinyl)-4-thiazolyl]phenyl]carbonyl]amino]cyclohexyl]carbonyl]-L-methioninolHCID 5767285086%

反応条件

温度80 °C

反応手順

100 mg (0.74 mmol) of L-methioninol was added to a solution of 250 mg (0.68 mmol) of 2-[4-[2-(4-methyl-1-piperazinyl)-4-thiazolyl]phenyl]-3-oxa-1-azaspiro[4.5]dec-1-en-4-one in 20 ml of dimethylformamide. After the mixture was stirred at 80° C. for 15 hours, the reaction solution was concentrated under reduced pressure, ethyl acetate was added thereto, and the mixture was successively washed with water, a saturated aqueous sodium hydrogencarbonate solution and saturated brine, followed by drying with anhydrous sodium sulfate. After the solvent was distilled off under reduced pressure, and diisopropyl ether was added to the residue to wash the crystal to obtain 319 mg (86%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08481725B2
出典データセットuspto-grants-2013_07
ORD IDord-fa3326ca2b774c608a65c4913075f958
出典メモuspto-grants-2013_07