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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2298594생성일: 2026년 10월 26일

Hydrazine hydrate (1:1) → N'-amino-5-methylsulfanyl-4-(4-phenyl-1,3-thiazol-2-yl)thiophene-2-carboximidamide

https://huagongshe.com/reaction/2298594

반응식

참여 물질

역할이름HCID투입량
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물5-Methylthio-4-(4-phenyl(1,3-thiazol-2-yl))thiophene-2-carbonitrileHCID 18537264—
용매EthanolHCID 702—
생성물N'-amino-5-methylsulfanyl-4-(4-phenyl-1,3-thiazol-2-yl)thiophene-2-carboximidamideHCID 17850364145%

반응 단계

5-Methylthio-4-(4-phenyl(1,3-thiazol-2-yl))thiophene-2-carbonitrile (100 mg, 0.32 mmol) as prepared in previous step was dissolved in EtOH (10 mL). To this solution hydrazine monohydrate (10 eq) was added and the mixture was heated at reflux for 3 h. The EtOH solution was concentrated down to 1 mL and water (2 mL) was added to this solution. This resulted in the formation of a white solid. The solid was collected by filtration washed with a small amount of water and dried under vacuum to give 50 mg (45%) of hydrazino[5-methylthio-4-(4-phenyl(1,3-thiazol-2-yl))(2-thienyl)]methanimine. 1H-NMR (CD3OD/CDCl3; 300 MHz) δ2.69 (s, 3H), 7.35-7.43 (m, 1H), 7.44-7.49 (m, 2H), 7.52 (s, 1H), 7.96-7.99 (m, 2), 8.10 (s, 1H). Mass spectrum (ESI, m/z): Calcd. for C15H14N4S3, 347.04 (M+H), found 347.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06492403B1
출처 데이터셋uspto-grants-2002_12
ORD IDord-e66313bc1edc41408ca961bb42437c08
출처 메모uspto-grants-2002_12