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HRID 20847作成日:2026年10月23日

Hydrochloric Acid → (+/-)-2-Chloro-N-[{1-[(cyclopropylmethyl)(methyl)amino]cyclopentyl}(phenyl)methyl]-3-(trifluoromethyl)benzamide hydrochloride

https://huagongshe.com/ja/reaction/20847

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物CyclopropanecarboxaldehydeHCID 123114—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物(+/-)-2-Chloro-N-[[1-(methylamino)cyclopentyl](phenyl)methyl]-3-(trifluoromethyl)benzamideHCID 59347824—
触媒Acetic AcidHCID 176—
溶媒1,2-DichloroethaneHCID 11—
溶媒Diethyl EtherHCID 3283—
溶媒DichloromethaneHCID 6344—
生成物(+/-)-2-Chloro-N-[{1-[(cyclopropylmethyl)(methyl)amino]cyclopentyl}(phenyl)methyl]-3-(trifluoromethyl)benzamide hydrochlorideHCID 68563672—

反応手順

To a solution (±)-2-chloro-N-[[1-(methylamino)cyclopentyl](phenyl)methyl]-3-(trifluoromethyl)benzamide E22 (143 g; 0.35 mmol), cyclopropanecarboxaldehyde (0.026 ml; 0.035 mmol) and acetic acid (3 drops) in 1,2-dichloroethane (10 ml) was added sodium triacetoxyborohydride (303 mg; 1.4 mmol). The resulting mixture was allowed to stir at room temperature under argon overnight. Then the reaction mixture was diluted with DCM (20 ml), washed with saturated potassium carbonate solution and brine, dried (Na2SO4) and evaporated in vacuo. The mixture was separated by column chromatography on silica gel using 20% ether in n-pentane to 2% methanol in ether. The oil obtained was treated with 1M HCl in ether to give the title product as an off white hydrochloride salt (0.054 g; 33%). Mass Spectrum (Electrospray LC/MS). Found 465 (MH+). C25H2835ClF3N2O requires 464. Ret. time: 2.30 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07745642B2
出典データセットuspto-grants-2010_06
ORD IDord-bb50d10ebc9c4dcabf14fd48f8eff140
出典メモuspto-grants-2010_06