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HRID 2306287作成日:2026年10月25日

Triethylamine → 3-cyclopentyl-2-(3,4-dichloro-phenyl)-N-(4,5,6,7-tetrahydrobenzothiazol-2-yl)-propionamide

https://huagongshe.com/reaction/2306287

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-Amino-4,5,6,7-tetrahydrobenzothiazoleHCID 18046—
反応物Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
反応物3-cyclopentyl-2-(3,4-dichlorophenyl)propanoic AcidHCID 2762725—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物3-cyclopentyl-2-(3,4-dichloro-phenyl)-N-(4,5,6,7-tetrahydrobenzothiazol-2-yl)-propionamideHCID 1201054279%

反応手順

A solution of 3-cyclopentyl-2-(3,4-dichlorophenyl)-propionic acid (50 mg, 0.17 mmol), benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate (83 mg, 0.19 mmol), triethylamine (0.048 mL, 0.34 mmol), and 2-amino-4,5,6,7-tetrahydrobenzothiazole (40 mg, 0.26 mmol) in dry N,N-dimethylformamide (1 mL) was stirred at 25° C. for 14 h. The reaction mixture was then diluted with water and ethyl acetate, and the layers were separated. The organic layer was sequentially washed with a 1N aqueous hydrochloric acid solution, a saturated aqueous sodium chloride solution, and water. The organic layer was dried over magnesium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 1/1 hexanes/ethyl acetate) afforded 3-cyclopentyl-2-(3,4-dichloro-phenyl)-N-(4,5,6,7-tetrahydro-benzothiazol-2-yl)-propionamide (56 mg, 79%) as a white solid: mp 170-171° C.; EI-HRMS m/e calcd for C21H24Cl2N2OS (M+) 422.0986, found 422.0982.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06441184B1
出典データセットuspto-grants-2002_08
ORD IDord-c9e1ac94f0cd4b4e81c81975c4877e30
出典メモuspto-grants-2002_08