Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Trifluoroacetic acid | HCID 6422 | — |
| Edukt | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 3-Methoxypropionic acid | HCID 134442 | — |
| Edukt | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | HCID 57393214 | HCID 57393214 | — |
Reaktionsschritte
To a mixture of A215 (0.020 g, 0.065 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.019 g, 0.098 mmol), 1-hydroxybenzotriazole (0.013 g, 0.098 mmol), and diisopropylethylamine (0.034 mL, 0.195 mmol) in anhydrous dimethylformamide (2 mL) was added 3-methoxypropionic acid (9.20 μL, 0.098 mmol). The reaction mixture was stirred at room temperature overnight (After ˜3 hr, the reaction mixture became homogenous). The solvent was removed under reduced pressure, and the residue was diluted with dichloromethane, washed with water, and dried over anhydrous sodium sulfate. Concentration under pressure followed by purification by flash silica gel chromatography using a 5% mixture of methanol in dichloromethane afforded 0.018 g (69%) of A216 as a yellow solid. The compound had an HPLC retention time=1.84 min. (Column: Chromolith SpeedROD 4.6×50 mm—4 min.; Solvent A=10% MeOH, 90% H2O, and 0.1% TFA; Solvent B=90% MeOH, 10% H2O, and 0.1% TFA) and a LC/MS M+1=394.37. 1H NMR (400 MHz, CDCl3) δ ppm 2.62 (t, J=7.15 Hz, 2 H) 3.15 (d, J=6.60 Hz, 3 H) 3.54 (s, 3 H) 3.78 (t, J=7.15 Hz, 2 H) 4.01 (s, 3 H) 4.56 (d, J=6.10 Hz, 2 H) 5.49-5.54 (m, 1 H) 6.96-6.98 (m, 2 H) 7.51-7.58 (m, 3 H) 9.98 (s, 1 H)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07737279B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-143b8358ec3a4888b04d3d892bb7d06c |
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| Quellennotiz | uspto-grants-2010_06 |
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