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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1455940생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1455940

반응식

참여 물질

역할이름HCID투입량
반응물BenzenesulfonamideHCID 7370—
반응물TriethylamineHCID 8471—
반응물1-(3-Dimethylaminopropyl)ethylcarbodiimide hydrochlorideHCID 21982921—
반응물2-[N-(2-benzyloxy-5-bromobenzyl)-N-ethylamino]thiazole-5-carboxylic acidHCID 22105530—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물2-[N-(2-benzyloxy-5-bromobenzyl)-N-ethylamino]-N-(phenylsulphonyl)thiazole-5-carboxamideHCID 22105582—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05843942
출처 데이터셋uspto-grants-1998_12
ORD IDord-598886c70a264870925ddd16e07dd090
출처 메모uspto-grants-1998_12