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HRID 341456作成日:2026年10月27日

3,3,3-Trifluoropropanal → 2-N-Methyl-2-N-phenyl-6-{5-[(2S)-1-(3,3,3-trifluoropropyl)pyrrolidin-2-yl]-1,2,4-oxadiazol-3-yl}-1,3,5-triazine-2,4-diamine

https://huagongshe.com/reaction/341456

反応式

関与物質

役割名称HCID仕込み量
反応物3,3,3-TrifluoropropanalHCID 68028—
反応物Sodium AcetateHCID 517045—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物2-N-methyl-2-N-phenyl-6-{5-[(2S)-pyrrolidin-2-yl]-1,2,4-oxadiazol-3-yl}-1,3,5-triazine-2,4-diamine hydrochlorideHCID 66802565—
溶媒1,2-DichloroethaneHCID 11—
溶媒DichloromethaneHCID 6344—
生成物2-N-Methyl-2-N-phenyl-6-{5-[(2S)-1-(3,3,3-trifluoropropyl)pyrrolidin-2-yl]-1,2,4-oxadiazol-3-yl}-1,3,5-triazine-2,4-diamineHCID 6680237619.4%

反応手順

To a solution of 2-N-methyl-2-N-phenyl-6-{5-[(2S)-pyrrolidin-2-yl]-1,2,4-oxadiazol-3-yl}-1,3,5-triazine-2,4-diamine hydrochloride (Example 438, 0.2 g, 0.535 mmol) in DCE (5 mL) was added sodium acetate (0.07 g, 0.8 mmol) and 3,3,3-trifluoropropanal (0.12 g, 1.070 mmol) and the mixture was stirred for 1 h at room temperature. Sodium triacetoxyborohydride (0.17 g, 0.8 mmol) was added and the reaction mixture was stirred for 2 h at room temperature. DCM was added and the mixture was washed with saturated aq. sodium bicarbonate, and then brine. The organic layer was dried over sodium sulfate and concentrated under vacuum. The residue was purified by FCC, eluting with 20-100% EtOAc in heptane to afford the title compound (0.045 g, 19%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895733B2
出典データセットuspto-grants-2014_11
ORD IDord-bcb1dbc97c884400b9c95defbcc88bec
出典メモuspto-grants-2014_11