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HRID 75116作成日:2026年10月25日

o-Methylvalerolactim → 3-(3,4-Difluorophenyl)-5,6,7,8-tetrahydroimidazo-[1,5-a]pyridine-1-carboxylic acid

https://huagongshe.com/reaction/75116

反応式

関与物質

役割名称HCID仕込み量
反応物o-MethylvalerolactimHCID 138567—
反応物Lithium hydroxide, monohydrateHCID 168937—
反応物2-(3,4-difluorophenyl)oxazol-5(4H)-oneHCID 58054172—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物3-(3,4-Difluorophenyl)-5,6,7,8-tetrahydroimidazo-[1,5-a]pyridine-1-carboxylic acidHCID 5805418571%

反応条件

温度90 °C

反応手順

6-methoxy-2,3,4,5-tetrahydropyridine (0.431 g, 3.80 mmol) was dissolved in THF (5 mL) in a 40 mL screw-cap vial and 2-(3,4-difluorophenyl)oxazol-5(4H)-one (0.75 g, 3.80 mmol) in THF (5 mL) was added, producing an orange solution. The vial was capped and heated to 90° C. for 3 hours. THF was removed under reduced pressure and the residue was dissolved in MeOH (10 ml) and lithium hydroxide monohydrate (0.479 g, 11.41 mmol) in water (1 mL) was added. The reaction was heated to 90° C. for 3 hours. MeOH was removed by evaporation under reduced pressure. The remaining aqueous solution was diluted with water (5 mL) and acidified to pH 2 with 5M HCl. The solution was extracted with EtOAc (3×5 mL). The combined organic extracts were dried over anhydrous sodium sulfate, filtered and evaporated to yield the desired product as a brown oil (742 mg, 71%) that was used without further purification. LCMS (+ESI) m/z: 279.3 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835422B2
出典データセットuspto-grants-2014_09
ORD IDord-6dfdf4e4b2b14b39b3030a94bfc4e3bf
出典メモuspto-grants-2014_09