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HRID 20844作成日:2026年10月25日

2,6-Dimethylbenzoic acid → 2,6-Dimethyl-N-[[1-(methylamino)cyclopentyl](phenyl)methyl]benzamide

https://huagongshe.com/reaction/20844

反応式

関与物質

役割名称HCID仕込み量
反応物2,6-Dimethylbenzoic acidHCID 12439—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
反応物{[Amino(phenyl)methyl]cyclopentyl}methylamineHCID 57444874—
溶媒DimethylformamideHCID 6228—
溶媒DiisopropylethylamineHCID 81531—
生成物2,6-Dimethyl-N-[[1-(methylamino)cyclopentyl](phenyl)methyl]benzamideHCID 1152288676%

反応手順

To a solution of 2,6-dimethylbenzoic acid (0.100 g; 0.668 mmol) in DMF (5 ml) and DIPEA (0.12 ml) was added {[amino(phenyl)methyl]cyclopentyl}methylamine D31 enantiomer 2 (0.124 g; 0.608 mmol) and HATU (0.254 g; 0.668 mmol). The resulting mixture was allowed to stir at room temperature for 3 days and then the DMF was evaporated off under reduced pressure. Residual material was partitioned between ethyl acetate and water, washed with water and the organic layer was dried (Na2SO4) and evaporated. The residual material was dissolved in DCM (2 ml) and loaded onto an SCX cartridge. Washing with DCM, then methanol followed by elution with 1 M ammonia in methanol afforded the title product (155 mg; 76%). 1H NMR (CDCl3) δ: 1.3-1.8 (9H, m), 2.21 (3H, s), 2.28 (6H, s), 5.07 (1H, m), 7.0 (2H, m), 7.1-7.4 (7H, m). Mass Spectrum (Electrospray LC/MS). Found 337 (MH+). C22H28N2O requires 336. Ret. time: 1.86 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-4d7b6c3ca3c241229878f9f0254ed117
出典メモuspto-grants-2010_06