Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phenyl chloroformate | HCID 15891 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 4-Methoxy-7-(tetrahydro-pyran-4-yl)-benzothiazol-2-yl-amine | HCID 22015735 | — |
| Edukt | (4-Methoxy-7-phenyl-benzothiazol-2-yl)-carbamic acid benzyl ester | HCID 86584926 | — |
| Edukt | HCID 178521615 | HCID 178521615 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | HCID 178488703 | HCID 178488703 | 7% |
Reaktionsschritte
4-Methoxy-7-(tetrahydro-pyran-4-yl)-benzothiazol-2-ylamine (69 mg, 0.26 mmol) is first reacted with phenyl chloroformate as described for (4-methoxy-7-phenyl-benzothiazol-2-yl)-carbamic acid benzyl ester in WO01/97786 and then with N-ethyl-diisopropylamine (0.090 ml, 0.52 mmol) and (trans)-cyclohexane-1,4-diol (60 mg, 0.52 mmol) in dimethyl sulfoxide (10 ml) at 50° C. for 2 h. Then 100 ml dichoromethane are added, the mixture is extracted with saturated aqueous sodium carbonate and the organic phase is dried and evaporated. Flash-chromatographic purification (silica, eluting with dichloromethane/methanol) yielded the title compound as white solid (7% yield). MS: m/e=407(M+H+), mp 282-284° C. Following the general method of example 1 the compounds of examples 2 to 11 were prepared.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07304058B2 |
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| Quelldatensatz | uspto-grants-2007_12 |
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| ORD ID | ord-11fd3b0b8d58482a8356e58c8abe301d |
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| Quellennotiz | uspto-grants-2007_12 |
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