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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 127403생성일: 2026년 10월 24일

Acetate → N-(1-allyl-2-pyrrolidylmethyl)-7-sulfamoyl-1,4-benzodioxane-5-carboxamide

https://huagongshe.com/ko/reaction/127403

반응식

참여 물질

역할이름HCID투입량
반응물AcetateHCID 175—
반응물1-(Allyl)pyrrolidine-2-methylamineHCID 117296—
반응물Methyl-7-sulfamoyl-1,4-benzodioxane-5-carboxylateHCID 20544687—
용매WaterHCID 962—
생성물N-(1-allyl-2-pyrrolidylmethyl)-7-sulfamoyl-1,4-benzodioxane-5-carboxamideHCID 2483492764.8%

반응 단계

145 g of methyl-7-sulfamoyl-1,4-benzodioxane-5-carboxylate, 48 g of water and 89 g of 1-allyl-2-aminomethyl-pyrrolidine were introduced into a balloon flask provided with a condenser. The mixture was heated on a water bath until a test sample was soluble in dilute acids and then 1 liter of water was added. The precipitated carboxamide was redissolved by acetate formation. The solution formed was filtered on carbon black and then the base was precipitated by the addition of 20% ammonia. The resulting crystals were dried off, washed with water, dried and purified by passing over hydrochloride (M.P.: 228°-230° C.) followed by transformation into a base by treatment with 20% ammonia. 131 g of N-(1-allyl-2-pyrrolidylmethyl)-7-sulfamoyl-1,4-benzodioxane-5-carboxamide was produced (M.P.: 143°-144° C.; yield: 64.8%). The structure was confirmed by nuclear magnetic resonance.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04255580
출처 데이터셋uspto-grants-1981_03
ORD IDord-d432ac23ca704fcdb426b3353b672908
출처 메모uspto-grants-1981_03