HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2080992Erstellt: 25. Oktober 2026
p-Toluenesulfonic acid monohydrate → HCID 178433271, Verbindung
https://huagongshe.com/reaction/2080992
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Edukt | N-[(2-Chloro-3,4-difluorophenyl)methyl]-3-methyl-2-oxo-4-imidazolidinecarboxamide | HCID 25098282 | — |
| Edukt | HCID 178433279 | HCID 178433279 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Produkt | HCID 178433271 | HCID 178433271 | 74% |
Reaktionsschritte
A solution of N-[(2-chloro-3,4-difluorophenyl)methyl]-3-methyl-2-oxo-4-imidazolidinecarboxamide (152 mg, 0.5 mmol) (prepared as described in Example 28), (4-methyl-1H-imidazol-5-yl)methanol hydrochloride (93 mg, 0.625 mmol) and p-toluene sulfonic acid monohydrate (19 mg, 0.100 mmol) in N-methyl-2-pyrrolidone (1 ml) was heated at 130° C. under argon for 3 h. The reaction mixture was cooled to room temperature and diluted with dichloromethane. The solution was washed with saturated sodium hydrogen carbonate solution and brine, dried and evaporated. The residue was purified by mass-directed automated HPLC, followed by trituration with ether to give N-[(2-chloro-3,4-difluorophenyl)methyl]-3-methyl-1-[(4-methyl-1H-imidazol-5-yl)methyl]-2-oxo-4-imidazolidinecarboxamide (147 mg, 74%). LC/MS [M+H]+=398, retention time=1.57 minutes.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07932282B2 |
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| Quelldatensatz | uspto-grants-2011_04 |
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| ORD ID | ord-07145fe5a9d647ceb0743b1767052f77 |
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| Quellennotiz | uspto-grants-2011_04 |
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