HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 349266Erstellt: 24. Oktober 2026
Hydrochloric Acid → 5-Amino-1-(3,5-bis-trifluoromethyl-benzyl)-1H-imidazole-4-carboxylic acid amide
https://huagongshe.com/de/reaction/349266
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 5-Aminoimidazole-4-carboxamide | HCID 9679 | — |
| Edukt | 1-(Chloromethyl)-3,5-bis(trifluoromethyl)benzene | HCID 123576 | — |
| Produkt | 5-Amino-1-(3,5-bis-trifluoromethyl-benzyl)-1H-imidazole-4-carboxylic acid amide | HCID 86601219 | — |
Reaktionsschritte
Wash sodium hydride (2.71 g of a 60% solution in mineral oil, 67.66 mmol) three times with hexanes, then dilute with 85 mL of DMF. To this mixture add the HCl salt of 5-amino-1H-imidazole-4-carboxylic acid amide (5.0 g, 30.75 mmol) neat in four portions. The mixture generates gas and remains cloudy and turns a slightly green color. After mixing for 40 min., add 1-chloromethyl-3,5-bis-trifluoromethyl-benzene (8.88 g, 33.83 mmol). (The mixture again generates gas and darkens). Stir at RT for 2 days, then pour through a plug of Celite and wash with DMF (50 mL) and xylenes (50 mL). Remove the DMF via azeotropic distillation with xylenes under reduced pressure (5×50 mL), and then concentrate the residue under a steady stream of nitrogen for 18 h to provide the title compound as a dark purple solid. MS (ES) 351.1, 353.1 (M+1); 1H NMR (300 MHz, CDCl3) δ 7.70 (s, 1H), 7.58 (s, 2H), 7.31 (s, 2H), 6.96 (s, 1H), 5.46 (s, 2H), 5.10 (s, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07179804B2 |
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| Quelldatensatz | uspto-grants-2007_02 |
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| ORD ID | ord-dd73dd882f0340b5a9de6a3b90c3a478 |
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| Quellennotiz | uspto-grants-2007_02 |
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