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HRID 277798作成日:2026年10月25日

1,1'-Carbonyldiimidazole → HCID 53880492、化合物

https://huagongshe.com/reaction/277798

反応式

関与物質

役割名称HCID仕込み量
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物1,2-Oxazole-5-carboxylic acidHCID 2060599—
反応物(S)-(-)-N-[[2-Oxo-3-[4-(4-piperidinyl)-3-fluorophenyl]-5-oxazolidinyl]methyl]acetamideHCID 15887422—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 53880492HCID 53880492—

反応手順

A solution of isoxazole-5-carboxylic acid (79 mg) and 1,1′-carbonyldiimidazole (80 mg) in dry tetrahydrofuran (2.0 mL) is stirred at ambient temperature for one hour, and a solution of (S)-(−)-N-[[2-oxo-3-[4-(4-piperidinyl)-3-fluorophenyl]-5-oxazolidinyl]methyl]acetamide (EXAMPLE 20, 150 mg) in dry tetrahydrofuran (6.0 mL) is added. The mixture is then stirred at ambient temperature for 19 hours, concentrated under reduced pressure, diluted with methylene chloride (20 mL), washed with saturated aqueous sodium bicarbonate (10 mL), water (10 mL) and saline (10 mL), dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the crude product which is chromagraphed on silica gel (70-230 mesh, 10 g), eluting with methanol/methylene chloride (7.5/92.5). Pooling and concentration of those fractions with an Rf=0.67 by TLC (methanol/chloroform, 10/90) and recrystallization from chloroforr/diethyl ether gives the title compound, mp 290-292° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06358942B1
出典データセットuspto-grants-2002_03
ORD IDord-40cf709a0c73435a9a8b1e41df43a113
出典メモuspto-grants-2002_03