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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 622336생성일: 2026년 10월 26일

Dimethylformamide → N-methyl-N-carboxymethylglycylthyroxine methyl ester

https://huagongshe.com/reaction/622336

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물TriethylamineHCID 8471—
반응물N-methyliminodiacetic acidHCID 20441—
반응물Methyl thyroxinate hydrochlorideHCID 13911220—
용매TetrahydrofuranHCID 8028—
생성물N-methyl-N-carboxymethylglycylthyroxine methyl esterHCID 2282770669%

반응 단계

In 15 ml. of dimethylformamide (DMF) was dissolved 2 g. of thyroxine methyl ester hydrochloride, and to this was added 500 μl. of triethylamine. After 10 min., 0.55 g. of N-methyliminodiacetic acid in 5 ml. of THF was added to the resulting solution. This reaction mixture was concentrated in a rotary evaporator, and a residue was dissolved in 50 ml. of THF. After addition of 150 ml. of ethyl acetate, the mixture was shaken. The ethyl acetate phase was taken up and washed successively with three portions of distilled water and one portion of a saturated aqueous saline solution. The ethyl acetate phase was dried over anhydrous sodium sulfate, and the supernatant was concentrated in a rotary evaporator. To the residue were successively added 20 ml. of THF and a small amount of n-hexane. The produced precipitate was collected by filtration with suction to obtain a white crystalline product. The product was dried in a vacuum desiccator to give white crystals; yield 69%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04771008
출처 데이터셋uspto-grants-1988_09
ORD IDord-ff0ecdfdccd34648b2e920c1ca5edf0a
출처 메모uspto-grants-1988_09