Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Chloride | HCID 312 | — |
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | 5-(Methoxycarbonyl)pyridine-2-carboxylic acid | HCID 314992 | — |
| Edukt | Tert-butyl 5-amino-3-[2-(3-methoxyphenyl)ethyl]pyrazole-1-carboxylate | HCID 57440385 | — |
| Katalysator | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Formic Acid | HCID 284 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | HCID 178497986 | HCID 178497986 | — |
Reaktionsschritte
5-Methoxycarbonylpyridine-2-carboxylic acid (0.285 g, 1.58 mmol) was added to DCM (40 ml), to this was added oxayl chloride (0.165 ml, 1.90 mmol) and a few drops of anhydrous DMF. The reaction mixture was stirred for 30 mins before the addition of tert-butyl 5-amino-3-[2-(3-methoxyphenyl)ethyl]pyrazole-1-carboxylate (0.50 g, 1.58 mmol) and pyridine (2.0 ml). The reaction was stirred overnight. The reaction was evaporated to dryness to give yield to a gum. To this gum was added formic acid. The reaction mixture was stirred for 1 h before being evaporated to dryness. The resulting gum was quenched with saturated potassium carbonate (30 ml), extracted with DCM (3×50 ml), dried (MgSO4) and the solvent removed in vacuo to yield a viscous gum. Trituration with acetonitrile gave the desired product as a slightly yellow solid (24 mg, 4%); 1H NMR (400.132 MHz, DMSO) δ 2.92 (s, 4H), 3.74 (s, 3H), 3.95 (s, 3H), 6.50 (s, 1H), 6.76 (d, 1H), 6.83-6.82 (m, 2H), 7.20 (t, 1H), 8.26 (d, 1H), 8.53 (d, 1H), 9.17 (s, 1H), 10.38 (s, 1H), 12.31 (s, 1H); MH+381.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08129391B2 |
|---|
| Quelldatensatz | uspto-grants-2012_03 |
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| ORD ID | ord-d1844e8730d445318e371f35b4c9f4c9 |
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| Quellennotiz | uspto-grants-2012_03 |
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