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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 357621생성일: 2026년 10월 23일

p-Toluenesulfonic acid → 1-[4-(Amidino)-2,3-dihydro-1H-inden-1-ylideneamino]-2-amino-4,5-di-hydro-imidazole dihydrochloride

https://huagongshe.com/ko/reaction/357621

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물Divinylbenzene-styreneHCID 174664—
반응물1,2-Diamino-4,5-dihydro-imidazole hydrochlorideHCID 18937940—
반응물1-Oxo-2,3-dihydro-1H-indene-4-carboximidamide--hydrogen chloride (1/1)HCID 18937943—
용매WaterHCID 962—
생성물1-[4-(Amidino)-2,3-dihydro-1H-inden-1-ylideneamino]-2-amino-4,5-di-hydro-imidazole dihydrochlorideHCID 69904385—

반응 단계

A solution of 0.24 g (0.001 mol) of 4-amidino-2,3-dihydro-1H-inden-1-one hydrochloride and 0.136 g (0.001 mol) of 1,2-diamino-4,5-dihydro-imidazole hydrochloride [m.p. 245°-246° C., prepared from the corresponding p-toluenesulfonate salt, see EP 0 327 919, Example 12, by ion exchange on ®Amberlite IRA-400 (anion exchanger based on a styrene/divinylbenzene polymer with quaternary ammonium groups in the Cl- form; Fluka, Buchs, Switzerland)] in 3 ml of water is left to stand at room temperature for 18 hours. The product that has crystallized out is filtered off with suction and recrystallized from water, yielding the title compound (monohydrate), m.p. 280° C. (decomp.), 1 H-NMR (DMSO/D2O): δ=8.17 (d, 1H); 7.66 (d, 1H); 7.54 (t, 1H); 4.18 (t, 2H); 3.70 (t, 2H); 3.25 (m, 2H); 3.13 (m, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05840911
출처 데이터셋uspto-grants-1998_11
ORD IDord-97b2d694d9664a8eaae5ae32eeeca138
출처 메모uspto-grants-1998_11