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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1388088생성일: 2026년 10월 26일

Hydrochloric Acid → N-acetyl-L-thyroxine N-(5-carboxypentyl)-carboxamide

https://huagongshe.com/reaction/1388088

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물6-Aminohexanoic AcidHCID 564—
반응물N-HydroxysuccinimideHCID 80170—
반응물Sodium BicarbonateHCID 516892—
반응물N-AcetylthyroxineHCID 20638380—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물N-acetyl-L-thyroxine N-(5-carboxypentyl)-carboxamideHCID 13171337823%

반응 단계

N-acetyl-L-thyroxine (Anal. Biochem., 33 (1970) 67) (1.0 g, 1.22 mmole) and N-hydroxysuccinimide (0.148 g, 1.28 mmole) are dissolved in 2 ml of dimethylformamide and 3 ml of tetrahydrofuran. Dicychlohexylcarbodiimide (0.264 g=1.28 mmole) is then added all at once and the reaction mixture stirred at room temperature for 4 hours. The dicyclohexylurea is removed by filtration and to the filtrate is added a solution of 6-aminocaproic acid (160 mg, 1.22 mmole) and sodium bicarbonate (204 mg, 2.44 mmole) in 1 ml of water. After stirring 2 hours the reaction mixture is acidified to pH 3 with 2 N HCl and extracted with methylene chloride. The organic extract is dried over magnesium sulfate and evaporated to the crude amide. Purification of the product is achieved by dissolving the crude material in methylene chloride containing a trace of methanol and precipitating the product with ether/hexane (75:25). The procedure is repeated two times to give 223 mg (23%) of pure product. It shows a single spot on TLC in 8% methanol in chloroform. The compound has the formula C22H24N2O6I4 and the following structure ##STR3##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04430263
출처 데이터셋uspto-grants-1984_02
ORD IDord-27bbf48fdcab4675a0cf51d5e72fdb62
출처 메모uspto-grants-1984_02