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HRID 1455940作成日:2026年10月27日

Benzenesulfonamide → 2-[N-(2-benzyloxy-5-bromobenzyl)-N-ethylamino]-N-(phenylsulphonyl)thiazole-5-carboxamide

https://huagongshe.com/reaction/1455940

反応式

関与物質

役割名称HCID仕込み量
反応物BenzenesulfonamideHCID 7370—
反応物TriethylamineHCID 8471—
反応物1-(3-Dimethylaminopropyl)ethylcarbodiimide hydrochlorideHCID 21982921—
反応物2-[N-(2-benzyloxy-5-bromobenzyl)-N-ethylamino]thiazole-5-carboxylic acidHCID 22105530—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物2-[N-(2-benzyloxy-5-bromobenzyl)-N-ethylamino]-N-(phenylsulphonyl)thiazole-5-carboxamideHCID 22105582—

反応手順

1-(3--Dimethylaminopropyl)ethylcarbodiimide hydrochloride (0.85 g) was added to a stirred mixture of 2-[N-(2-benzyloxy-5-bromobenzyl)-N-ethylamino]thiazole-5-carboxylic acid (1 g), benzenesulphonamide (0.35 g), 4-dimethylaminopyridine (0.27 g) and triethylamine (0.225 g) in N,N-dimethylformamide (100 mL) and the mixture was stirred at ambient temperature for 16 hours. Water (30 mL) was added to the reaction mixture which was then extracted three times with ethyl acetate (20 mL each time). The combined ethyl acetate extracts were washed consecutively with aqueous 2N HCL (3×10 mL), aqueous saturated NaHCO solution (3×10 mL) and water (10 mL) and dried. The residue obtained on evaporation of the solvent was filtered through silica using ethyl acetate as eluant. The solvent was evaporated and on trituration with diethyl ether the residue gave 2-[N-(2-benzyloxy-5-bromobenzyl)-N-ethylamino]-N-(phenylsulphonyl)thiazole-5-carboxamide, yield 0.358 g, mp 140°-145° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05843942
出典データセットuspto-grants-1998_12
ORD IDord-598886c70a264870925ddd16e07dd090
出典メモuspto-grants-1998_12