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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 22474생성일: 2026년 10월 24일

Dimethylformamide → (2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-methoxyiminoacetyl chloride

https://huagongshe.com/ko/reaction/22474

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Oxalyl chlorideHCID 65578—
반응물2-(5-Amino-1,2,4-thiadiazol-3-yl)-2-(methoxyimino)acetic acidHCID 10130412—
용매TetrahydrofuranHCID 8028—
생성물(2Z)-2-(5-amino-1,2,4-thiadiazol-3-yl)-2-methoxyiminoacetyl chlorideHCID 10198354—

반응 단계

In 30.0 ml of tetrahydrofuran (THF), 10.0 g of 2-(5-amino-1,2,4-thiadiazol-3-yl)-2(Z)-methoxyiminoacetic acid were stirred at -20° C., followed by the dropwise addition of a chlorinating reagent, which had been prepared beforehand by gradually adding 6.97 g of oxalyl chloride at 5° C. to a mixture of 100 ml of THF and 4.0 g of N,N-dimethylformamide (DMF) and then reacting them for 30 minutes. After they were reacted for 5 minutes, the reaction mixture was poured into 250 ml of ice water to precipitate crystals. The crystals were collected by filtration and washed with 100 ml of ice water. The resulting crystals were thereafter suspended in water and the suspension was adjusted to pH 4.0 with a 1M aqueous solution of sodium acetate. The resulting solution was extracted with 250 ml of ethyl acetate. The organic layer was dried over magnesium sulfate, followed by filtration. The filtrate was concentrated and, under reduced pressure, was then dried, whereby the title compound was obtained. Yield: 7.5 g (68.7%). Purity: 98.7 %.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05428173
출처 데이터셋uspto-grants-1995_06
ORD IDord-3ce216c8344a4ad0a3b0aeeb16824aef
출처 메모uspto-grants-1995_06