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HRID 36503作成日:2026年10月23日

L-Leucine → N-[2-[(Acetylthio)methyl]-3,3,3-trifluoro-1-oxopropyl]-L-leucine

https://huagongshe.com/ja/reaction/36503

反応式

関与物質

役割名称HCID仕込み量
反応物L-LeucineHCID 6106—
反応物Ethyl AcetateHCID 8857—
反応物N,N-Bis(trimethylsilyl)trifluoroacetamideHCID 65279—
反応物2-Trifluoromethyl-3-acetylthiopropionyl chlorideHCID 54308536—
溶媒Acetic AcidHCID 176—
溶媒MethanolHCID 887—
溶媒AcetonitrileHCID 6342—
溶媒HexaneHCID 8058—
生成物N-[2-[(Acetylthio)methyl]-3,3,3-trifluoro-1-oxopropyl]-L-leucineHCID 54059189—

反応手順

A stirred suspension of L-leucine (2.62 g., 20 mmol) in 35 mL of dry acetonitrile under argon was cooled to 0°-5° C. and bis(trimethylsilyl)trifluoroacetamide (10.62 mL, 40 mmol) was added. The reaction mixture was allowed to stir while slowly warming to room temperature. After 2 hours, another 3.5 mL (13 mmol) of bis(trimethylsilyl)trifluoroacetamide was added which resulted in a clear lemon color solution on additional stirring for one hour at room temperature. The reaction mixture was cooled to 0°-5° C. and 2-trifluoromethyl-3-acetylthiopropionyl chloride (4.69 g., 20 mmol.) dissolved in 8 mL of acetonitrile was added dropwise over 45 minutes. After stirring for 1.5 hours at 0°-5° C. to room temperature, TLC shows completion of the reaction. The reaction mixture was evaporated under reduced pressure to give a yellow oily residue which was partitioned between ethyl acetate (75 mL) and water (50 mL). The aqueous phase was further extracted with ethyl acetate (4×50 mL), the combined extracts were washed with 75 mL of brine, dried (MgSO4), and evaporated to give 10.3 g. of a yellow semi-solid residue. A 0.68 g. portion of this crude material was flash chromatographed on 75 g. of silica gel eluting with ethyl acetate: hexanes:acetic acid, 100:100:1 to yield 0.15 g. of the faster eluting diastereomer (isomer A) and 0.12 g. of slower eluting diastereomer (isomer B). The remaining 9.6 g. of crude material was flash chromatographed similarly (silica gel, 1300 g.) which gave 2.5 g. of isomer A, 2.7 g. of a mixture of both the diastereomers, and 1.5 g. of isomer B. The mixed fractions were rechromatographed using the same conditions to give 0.5 g. of isomer A and 1.25 g. of isomer B. Both the 2.5 g. and 0.5 g. portions of isomer A were combined, triturated with hexanes containing a few drops of ethyl acetate, filtered, and dried to yield 2.57 g. of the title isomer A product as a white crystalline solid, m.p. 150°-152° C., TLC Rf =0.40 (100:50:1 ethyl acetate:hexane:acetic acid), [α]D =-146.9° (c=1.00, methanol).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05414013
出典データセットuspto-grants-1995_05
ORD IDord-19b50f2930ac4e8b804301afa1f6a7e1
出典メモuspto-grants-1995_05