HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50773Erstellt: 26. Oktober 2026
Carbon Dioxide → 4-{[(Tert-butoxy)carbonyl]amino}pyridine-3-carboxylic acid
https://huagongshe.com/reaction/50773
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Carbon Dioxide | HCID 280 | — |
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | 4-(Boc-amino)pyridine | HCID 9990210 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4-{[(Tert-butoxy)carbonyl]amino}pyridine-3-carboxylic acid | HCID 22172623 | 54% |
Reaktionsschritte
n-Butyl lithium (2.18 M, 24 mL, 52.51 mmol) is added slowly to a solution of 4-(N-t-butoxycarbonylamino)-pyridine (4.08 g, 21 mmol) in THF (50 mL, stirred under N2 at −78° C. The solution is allowed to warm to 0° C., stirred for 3 h, then cooled again to −78° C. and poured into ether (100 mL) containing dry ice. The solution is warmed to room temperature with constant stirring. Water is added and the mixture is neutralized with acetic acid. The resulting solid is collected by vacuum filtration and dried in a vacuum oven to give 4-(N-t-butoxycarbonylamino)nicotinic acid (2.72 g, 54%) as a brown solid. 1H NMR (DMSO) δ 11.75 (1H, brs), 8.95 (1H, s), 8.50 (1H, d, J=6.0 Hz) 8.20 (1H, d, J=6.0 Hz), 1.49 (9H, s).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06713484B2 |
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| Quelldatensatz | uspto-grants-2004_03 |
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| ORD ID | ord-b4e7f44004264174a2fd5c2c996aaf75 |
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| Quellennotiz | uspto-grants-2004_03 |
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