Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Diethylcyanamide | HCID 12050 | — |
| Edukt | 3-(Adamant-1-yl)-1-(4-amino-2-methoxybenzenesulfonyl)-5-ethoxy-1,3-dihydro-2H-benzimidazol-2-one | HCID 23364275 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | HCID 178465975 | HCID 178465975 | — |
Reaktionsschritte
A mixture of 1.5 g of the compound obtained in EXAMPLE 40 step B), 1.5 g of N,N-diethylcyanamide, 20 ml of AcOEt and 3 ml of a 20% solution of HCl in EtOH is refluxed for 22 hours. 2 g of N,N-diethylcyanamide and 3 ml of a 20% solution of HCl in EtOH are then added and reflux is continued for 5 hours. After cooling, the reaction mixture is extracted with AcOEt, the organic phase is washed with water, with a 1N solution of NaHCO3 and with water and dried over Na2SO4 and the solvent is evaporated off under vacuum. The residue is chromatographed on silica using a DCM/AcOEt mixture (94/6; v/v) as the eluent. The product obtained is dissolved in EtOH, 1 ml of concentrated HCl is added and the mixture is evaporated under vacuum to give 0.2 g of the hydrochloride of the expected product after crystallization from an EtOH/ether mixture (50/50; v/v). M.p.=186° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05585394 |
|---|
| Quelldatensatz | uspto-grants-1996_12 |
|---|
| ORD ID | ord-86b211b04b374aaeafe2b1d3e51278e3 |
|---|
| Quellennotiz | uspto-grants-1996_12 |
|---|