Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Borane | HCID 6331 | — |
| Edukt | 2-(4-Morpholinylcarbonyl)-1,3-thiazol-5-amine | HCID 22397226 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-(Morpholin-4-ylmethyl)-1,3-thiazol-5-amine | HCID 22397141 | 35,2% |
Reaktionsschritte
To a solution of 2-(4-morpholinylcarbonyl)-1,3-thiazol-5-amine (Preparation 26, 1.0 g) in THF (10 mL) under nitrogen at ambient temperature is added borane (1.0 M solution in THF, 9.39 mL). The bright yellow mixture is heated to reflux (85° C.) for 1 h. The mixture is cooled to ambient temperature, quenched with aq. NH4Cl, and extracted with EtOAc (3×75 mL). The organic layer is dried (MgSO4) and the solvent removed. The residue is purified by column chromatography (eluent 2% MeOH/CH2Cl2) to afford 329 mg (35%) of the title compound as a yellow oil. Physical characteristics: 1H NMR (CDCl3) δ 2.49, 3.61, 3.65, 6.84; MS (ESI+) m/z 200 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06559145B2 |
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| Quelldatensatz | uspto-grants-2003_05 |
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| ORD ID | ord-e59034d651c340d6b5cc477239038f4a |
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| Quellennotiz | uspto-grants-2003_05 |
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