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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 460338생성일: 2026년 10월 24일

Hydrazine → HCID 178486503, 화합물

https://huagongshe.com/ko/reaction/460338

반응식

참여 물질

역할이름HCID투입량
반응물HydrazineHCID 9321—
반응물3-Fluorophenyl isothiocyanateHCID 9834—
반응물5,6-Dimethoxy-1-indanoneHCID 75018—
반응물Lithium hexamethyldisilaneHCID 57425481—
용매Acetic AcidHCID 176—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물HCID 178486503HCID 178486503—

반응 단계

A mixture of 5,6 dimethoxyindan-1-one, Compound 3a, (3.0 g, 0.0154 mole), 3-fluoro-phenyl isothiocyanate, Compound 4a, (2.4 g, 0.0157 mole) and THF (3.0 mL) was added to lithium hexamethyldisilane (15.4 mL, 0.0154 mole) dropwise at room temperature with stirring. The reaction mixture was stirred for 12 hrs. Hydrazine (0.75 mL, 0.0154 mole) and acetic acid (0.96 mL) were added to the reaction mixture, which was then heated at the reflux temperature for 24 hrs. The resulting mixture was first added to water (30 mL) and then extracted with CH2Cl2. The organic layers were combined and washed with aqueous NaHCO3 solution, then washed with water and brine solution, dried (Na2SO4), and solvent was removed in vacuo. The residue was dissolved in hot CH3CN. To the mixture was then added one equivalent of an HCl-ether solution to yield a precipitate of the title compound. The precipitate was dissolved in CH3CN and decolorized with charcoal and re-crystallized to give Compound 14 as an off white solid. MS m/z 326 (M+H)+; 1HNMR (DMSO-d6): 3.44(s, 2H), 3.80(s, 3H), 3.81(s, 3H),6.58(t, 1H),6.85 (d, 1H), 7.1(d, 1H), 7.21(s, 1H), 7.23(s, 1H), 7.3(m, 1H), 9.2(br s, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07196110B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-7b1b746452624cf3b25f7366049bbc14
출처 메모uspto-grants-2007_03