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HRID 2422712作成日:2026年10月25日

Trimethylaluminum → (R,R)-N-[3-(3-fluoro-4-methoxyphenyl)isothiazol-5-yl]-2-methylcyclopropane-carboxamide

https://huagongshe.com/reaction/2422712

反応式

関与物質

役割名称HCID仕込み量
反応物TrimethylaluminumHCID 16682925—
反応物HCID 67180743HCID 67180743—
反応物3-(3-Fluoro-4-methoxyphenyl)isothiazol-5-ylamineHCID 67181531—
溶媒Hydrochloric AcidHCID 313—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物(R,R)-N-[3-(3-fluoro-4-methoxyphenyl)isothiazol-5-yl]-2-methylcyclopropane-carboxamideHCID 6718063955.9%

反応手順

Add benzyl (R,R)-2-methylcyclopropanecarboxylate (0.55 g, 2.89 mmol) to a 0° C. solution of 3-(3-fluoro-4-methoxyphenyl)isothiazol-5-ylamine (0.59 g, 2.63 mmol) and trimethylaluminum (2.0 M in toluene, 5.26 mmol) in dichloromethane (5 mL) and allow reaction to naturally warm to room temperature. Warm the reaction mixture to 40° C. and allow to stir overnight. Dilute the reaction mixture with EtOAc (100 mL) and 1 N HCl (40 mL) and water (100 mL), collect the organic phase, and evaporate. Chromatography over silica gel eluting with 25-50% EtOAc in hexane affords (R,R)—N-[3-(3-fluoro-4-methoxyphenyl)isothiazol-5-yl]-2-methylcyclopropane-carboxamide. Yield: 55.9%. ES-MS: m/e 307.0 (m+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07960419B2
出典データセットuspto-grants-2011_06
ORD IDord-01de0d1aa4eb42cab0a9171a09706d32
出典メモuspto-grants-2011_06