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HRID 20849作成日:2026年10月24日

Dicyclohexylcarbodiimide → 4-Chloro-N-[[1-(dimethylamino)cyclopentyl](phenyl)methyl]-2-methylbenzamide

https://huagongshe.com/ja/reaction/20849

反応式

関与物質

役割名称HCID仕込み量
反応物DicyclohexylcarbodiimideHCID 10868—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物4-Chloro-2-methylbenzoic acidHCID 348269—
反応物Sodium BicarbonateHCID 516892—
反応物{1-[Amino(phenyl)methyl]cyclopentyl}dimethylamineHCID 11521393—
反応物(+/-)N-[[3-(Dimethylamino)tetrahydro-3-furanyl](phenyl)methyl]-2,6-dimethylbenzamideHCID 59347760—
溶媒DichloromethaneHCID 6344—
生成物4-Chloro-N-[[1-(dimethylamino)cyclopentyl](phenyl)methyl]-2-methylbenzamideHCID 5934778243%

反応手順

A mixture of {1-[amino(phenyl)methyl]cyclopentyl}dimethylamine D3 enantiomer 2 (80 mg, 0.37 mmol), 4-chloro-2-methylbenzoic acid (68 mg; 0.40 mmol), HOBt (61 mg; 0.40 mmol) and PS-DCC (310 mg of 1.3 mmol/g loading, 0.40 mmol) in DCM (4 ml) was shaken overnight. Saturated aqueous sodium bicarbonate was added and the mixture separated with a phase-sep cartridge and the organics applied directly to SCX resin. Elution with DCM, methanol and then 1M ammonia in methanol, followed by chromatography eluting with 12-100% ethyl acetate-pentane (SP4 Biotage) afforded the title product (64 mg; 43%). 1H NMR (CDCl3) δ: 0.9-1.0 (1H, m), 1.25-1.40 (1H, m), 1.4-1.6 (2H, m), 1.6-1.75 (2H, m), 1.8-1.9 (2H, m), 2.22 (6H, s), 2.41 (3H, s), 5.09 (1H, d, J=5 Hz), 7.07 (1H, d, J=5 Hz), 7.2-7.4 (8H, m). Mass Spectrum (Electrospray LC/MS): Found 371 (MH+). C22H2735ClN2O requires 370. Ret. time 2.26 min. The title product was converted to the corresponding hydrochloride salt.

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-b47023f147ae4c59b1d092eef245a220
出典メモuspto-grants-2010_06