HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 251070Erstellt: 26. Oktober 2026
Potassium Carbonate → {4-[(3-Fluoro-pyridin-2-ylmethyl)-amino]-butyl}-methyl-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/251070
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | N-(4-Aminobutyl)-N-methyl carbamic acid tert-butyl ester | HCID 2756377 | — |
| Edukt | Sodium borohydride | HCID 4311764 | — |
| Edukt | 3-Fluoro-2-pyridinecarboxaldehyde | HCID 11344017 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | {4-[(3-Fluoro-pyridin-2-ylmethyl)-amino]-butyl}-methyl-carbamic acid tert-butyl ester | HCID 67271861 | 74% |
Reaktionsschritte
A mixture of (4-amino-butyl)-methyl-carbamic acid tert-butyl ester (0.202 g, 1.00 mmol), 3-fluoro-pyridine-2-carbaldehyde (0.125 g, 1.00 mmol) and K2CO3 (0.138 g, 1.00) in MeOH (5 mL) was stirred for 16 h. The mixture was filtered through a celite cake and NaBH4 (0.050 g, 1.3 mmol) was added to the filtrate, and the mixture was stirred for 30 min. Saturated aqueous NaHCO3 (20 mL) was added, and MeOH was removed. The aqueous residue was extracted with CH2Cl2 (3×30 mL). The organic extracts were combined and dried over anhydrous Na2SO4. After filtration the solvent was removed by evaporation under vacuum, and the residue was purified by flash chromatography on a silica gel column (50:2:1 CH2Cl2/MeOH/NH4OH), affording {4-[(3-fluoro-pyridin-2-ylmethyl)-amino]-butyl}-methyl-carbamic acid tert-butyl ester as a colorless oil (0.230 g, 74%). 1H NMR (CDCl3) δ 1.42 (s, 9H), 1.48-1.54 (m, 4H), 2.61-2.68 (m, 2H), 2.80 (s, 3H), 3.14-3.22 (m, 2H), 3.96 (s, 2H), 7.11-7.20 (m, 1H), 7.30-7.36 (m, 1H), 8.33-8.38 (m, 1H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07863293B2 |
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| Quelldatensatz | uspto-grants-2011_01 |
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| ORD ID | ord-c56fed248a64434cb85fd83a053f079e |
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| Quellennotiz | uspto-grants-2011_01 |
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