Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Acetic Acid | HCID 176 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | 1-Butanaminium, N,N,N-tributyl-, fluoride, hydrate | HCID 16211673 | — |
| Edukt | HCID 178447258 | HCID 178447258 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | HCID 178437174 | HCID 178437174 | 86,7% |
Reaktionsschritte
To a mixture of 5.0 g (15.1 mmol) of N-[4-hydroxy-5-(trimethylsilyl) ethynyl-7H-pyrrolo[2,3-d]pyrimidin-2-yl]-2,2-dimethylpropionamide, in 40 mL of DMF and 10 mL of tetrahydrofuran was added 6.6 g (15.1 mmol) of tetrabutylammonium fluoride hydrate and the resulting solution was stirred at ambient temperature for 3.5 hours. After addition of 1.18 g of acetic acid and stirring for 15 minutes the mixture was poured into 50 mL of water. After stirring for about 1 hour the resulting suspension was filtered and the precipitate washed with water and dried, affording 3.38 g (86%) of N-(4-hydroxy-5-ethynyl-7H-pyrrolo[2,3-d]pyrimidin-2-yl)-2,2-dimethylpropionamide, mp>300° C. NMR δ1.21 (s, 9H) , 3.89 (s, 1H), 7.28 (s, 1H), 10.82 (br s, 1H), 11.82 (br s, 1H), 11.85 (br s, 1 H); IR (KBr) 3354, 3250, 2973, 2120, 1699, 1676, 1608, 1536, 1433, 1243 cm-1 ; UV (EtOH) 292 nm (ε13,900), 280 nm (ε14,500), 236 nm (ε14,900). Anal. Calcd for C13H14N4O2 : C, 60.46; H, 5.46; N, 21.69. Found: C, 60.25; H, 5.32; N, 21.49.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US05426187 |
|---|
| Quelldatensatz | uspto-grants-1995_06 |
|---|
| ORD ID | ord-1a9dd9ab671e4cde9c3bad0659bb4deb |
|---|
| Quellennotiz | uspto-grants-1995_06 |
|---|