HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 244864Erstellt: 24. Oktober 2026
4-Toluenesulfonyl chloride → N-[4-amino-2-(ethoxymethyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-8-yl]-2-methylpropanamide
https://huagongshe.com/de/reaction/244864
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Edukt | Ammonium Hydroxide | HCID 14923 | — |
| Edukt | m-Chloroperbenzoic acid | HCID 70297 | — |
| Edukt | N-[2-(ethoxymethyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-8-yl]-2-methylpropanamide | HCID 69077219 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Produkt | N-[4-amino-2-(ethoxymethyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-8-yl]-2-methylpropanamide | HCID 57657238 | — |
Reaktionsschritte
3-Chloroperoxybenzoic acid (60% pure, 0.283 g, 1.0 mmol) was added to a solution of N-[2-(ethoxymethyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-8-yl]-2-methylpropanamide (0.380 g, 1.0 mmol) in chloroform (10 mL) and the reaction was stirred for 1 hour. The mixture was cooled in an ice bath and ammonium hydroxide (3 mL) was added. After 15 minutes of stirring, p-toluenesulfonyl chloride (0.190 g, 1.0 mmol) was added and the reaction mixture was stirred for 72 hours. The fractions were separated and the aqueous fraction was extracted with chloroform. The combined organic fractions were washed with brine and purified by chromatography using a HORIZON HPFC system (silica cartridge, eluting with a linear gradient of 2-20% CMA in chloroform). Recrystallization from acetonitrile provided 0.231 g of N-[4-amino-2-(ethoxymethyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-8-yl]-2-methylpropanamide as an off-white solid, mp 259-261° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08658666B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-f8a6b5cbb6b64915903855bdcfe78e0e |
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| Quellennotiz | uspto-grants-2014_02 |
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