HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1870921Erstellt: 23. Oktober 2026
Triphosgene → Methyl 1,3-dihydro-4-methyl-2-oxo-thieno[3,4-d]imidazole-6-carboxylate
https://huagongshe.com/de/reaction/1870921
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triphosgene | HCID 94429 | — |
| Edukt | Methyl 3,4-diamino-5-methylthiophene-2-carboxylate | HCID 18693138 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Methyl 1,3-dihydro-4-methyl-2-oxo-thieno[3,4-d]imidazole-6-carboxylate | HCID 18693187 | 4.777,4% |
Reaktionsschritte
Methyl 3,4-diamino-5-methylthiophene-2-carboxylate (3.0 g) was dissolved in a mixture of N,N-dimethyl formamide (5 ml) and dichloromethane (15 ml). To the solution was added triphosgene (2.4 g) in portions. The mixture was stirred for two days at room temperature, and precipitates were collected by filtration, washed with dichloromethane and dried. Resultant white powder (2.4 g) was suspended in N,N-dimethylformamide (25 ml). To the suspension was added sodium hydride (60% in oil; 0.55 g), and the mixture was stirred for three days at room temperature. The solvent was evaporated under reduced pressure. To the residue was added 2N-HCl. Resulting precipitates were collected by filtration, washed with water, ether and methanol successively, followed by drying to afford the title compound (82 g, 53%) as pale brown powder.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06100252 |
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| Quelldatensatz | uspto-grants-2000_08 |
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| ORD ID | ord-fa368a6f8ed04cd79d82b177fe8d5de0 |
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| Quellennotiz | uspto-grants-2000_08 |
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