HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1519478Erstellt: 26. Oktober 2026
Trimethylamine → (2-{7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yloxycarbonylamino}-ethyl)-trimethyl-ammonium chloride
https://huagongshe.com/reaction/1519478
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Trimethylamine | HCID 1146 | — |
| Edukt | {7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl} (2-chloroethyl)carbamate | HCID 86708937 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | (2-{7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yloxycarbonylamino}-ethyl)-trimethyl-ammonium chloride | HCID 66733336 | — |
Reaktionsschritte
Trimethylamine (30% solution, 0.5 ml) was added to an ethanol solution (10 ml) of {7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl}(2-chloroethy)carbamate (330 mg), and the mixture was heated at 170° C. for 15 minutes (microwave reactor). After cooling to room temperature, the reaction mixture was concentrated under reduced pressure. To the residue was added ethyl acetate, and the resulted precipitates were collected by filtration and dried to obtain 120 mg of (2-{7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yloxycarbonylamino}-ethyl)-trimethyl-ammonium chloride as white powder.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09073868B2 |
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| Quelldatensatz | uspto-grants-2015_07 |
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| ORD ID | ord-67a158e7e0af4212bfc2efd29c842dd4 |
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| Quellennotiz | uspto-grants-2015_07 |
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