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HRID 490136作成日:2026年10月25日

Sodium Fluoride → tert-butyl(2S)-2-(azetidin-1-ylcarbonyl)-4-fluoropyrrolidine-1-carboxylate

https://huagongshe.com/reaction/490136

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium FluorideHCID 5235—
反応物Potassium CarbonateHCID 11430—
反応物N,N-Diethyl-1,1,2,3,3,3-hexafluoropropylamineHCID 136149—
反応物tert-butyl(2S,4S)-2-(azetidin-1-ylcarbonyl)-4-hydroxypyrrolidine-1-carboxylateHCID 67429167—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物tert-butyl(2S)-2-(azetidin-1-ylcarbonyl)-4-fluoropyrrolidine-1-carboxylateHCID 67429147—

反応手順

2.68 g of a mixture (approximately 3:1) of 1,1,2,3,3,3-hexafluoro-1-(diethylamino)propane and 1,2,3,3,3-pentafluoro-1-(diethylamino)-2-propene was added dropwise over a period of 10 minutes under ice cooling to a suspension of 2.71 g of the compound obtained in step 7-1 and 505 mg of sodium fluoride in 27 mL of dichloromethane, after which the reaction mixture was stirred for 16 hours at room temperature. 100 mL of a 5% potassium carbonate aqueous solution was added under ice cooling to the reaction solution, and the reaction mixture was stirred for 30 minutes at the same temperature. After liquid separation, the aqueous layer thus obtained was extracted with chloroform (30 mL×2), and the combined organic layer was washed with 50 mL of saturated brine and dried with magnesium sulfate, after which the drying agent was filtered off and the solvent was distilled off under reduced pressure. The residue thus obtained was subjected to column chromatography (silica gel 60, mobile phase: ethyl acetate) to obtain 2.30 g of the titled compound (colorless oil).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07528124B2
出典データセットuspto-grants-2009_05
ORD IDord-6f9469ed3f7f4ba4be928fc143428627
出典メモuspto-grants-2009_05