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HRID 357621作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物Divinylbenzene-styreneHCID 174664—
反応物1,2-Diamino-4,5-dihydro-imidazole hydrochlorideHCID 18937940—
反応物1-Oxo-2,3-dihydro-1H-indene-4-carboximidamide--hydrogen chloride (1/1)HCID 18937943—
溶媒WaterHCID 962—
生成物1-[4-(Amidino)-2,3-dihydro-1H-inden-1-ylideneamino]-2-amino-4,5-di-hydro-imidazole dihydrochlorideHCID 69904385—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05840911
出典データセットuspto-grants-1998_11
ORD IDord-97b2d694d9664a8eaae5ae32eeeca138
出典メモuspto-grants-1998_11