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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49738생성일: 2026년 10월 25일

Water → HCID 178475875, 화합물

https://huagongshe.com/reaction/49738

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물3-[3-(2-Cyanophenylsulfonyloxy)-5-methylphenoxy]propionaldehydeHCID 22722409—
반응물HCID 178513186HCID 178513186—
용매EthanolHCID 702—
생성물HCID 178475875HCID 178475875151%

반응 단계

[2-[3-(2-Cyanophenylsulfonyloxy)-5-methylphenoxy]ethyl-1-methylene]ydrazinecarboximidamide hydrochloride: A solution of 3-[3-(2-cyanophenylsulfonyloxy)-5-methylphenoxy]propionaldehyde (240 mg, 0.7 mmol), as prepared in the preceding step, and aminoguanidine nitrate (200 mg, 1.5 mmol) in ethanol (8 mL) was stirred at ambient temperature overnight. Water (20 mL) was added to the reaction mixture. The precipitates were collected, washed with water (2×15 mL) and diethyl ether (2×20 mL), and dried under high vacuum. The solid was suspended in water (40 mL), treated with 2N sodium hydroxide (1.0 mL), and extracted into dichloromethane (3×50 mL). The organic phase was dried over K2CO3. After removing the solvent, the residue was dissolved in dichloromethane (1 mL), and the dichloromethane solution was added to the solution of 1.5 mL of 0.6M HCl methanol in diethyl ether (50 mL) to give the title compound as a colorless solid (245 mg, 80%). 1H-NMR (300 MHz, DMSO-d6) δ 8.28 (m, 1H), 8.09 (m, 1H), 7.97-8.04 (m, 2H), 7.55 (br s, 5 H), 6.80 (s, 1H), 6.50 (s, 2H), 4.15 (t, J=6.3 Hz, 2H), 2.68 (m, 2H), 2.22 (s, 3H). Mass spectrum (MALDI-TOF, α-cyano-4-hydroxycinnamic acid matrix) calcd. for C18H19N5O4S: 402.1 (M+H), 424.1 (M+Na), 440.1 (M+K). Found: 402.1, 424.1, 440.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06706765B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-3202634c247040a78607862f492e95b4
출처 메모uspto-grants-2004_03