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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | p-Toluenesulfonic acid | HCID 6101 | — |
| 反応物 | Divinylbenzene-styrene | HCID 174664 | — |
| 反応物 | 1,2-Diamino-4,5-dihydro-imidazole hydrochloride | HCID 18937940 | — |
| 反応物 | 1-Oxo-2,3-dihydro-1H-indene-4-carboximidamide--hydrogen chloride (1/1) | HCID 18937943 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 1-[4-(Amidino)-2,3-dihydro-1H-inden-1-ylideneamino]-2-amino-4,5-di-hydro-imidazole dihydrochloride | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05840911 |
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| 出典データセット | uspto-grants-1998_11 |
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| ORD ID | ord-97b2d694d9664a8eaae5ae32eeeca138 |
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| 出典メモ | uspto-grants-1998_11 |
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