HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 243622Erstellt: 25. Oktober 2026
Hydrochloric Acid → Octanedioic acid hydroxyamide [4-(2-amino-phenyl)-thiazol-2-yl]-amide
https://huagongshe.com/reaction/243622
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Stannous Chloride | HCID 24479 | — |
| Edukt | Octanedioic acid benzyloxy-amide [4-(2-nitro-phenyl)-thiazol-2-yl]-amide | HCID 89972899 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Octanedioic acid hydroxyamide [4-(2-amino-phenyl)-thiazol-2-yl]-amide | HCID 25032253 | 53,2% |
Reaktionsschritte
To a mixture of compound 15 (0.040 g, 0.083 mmol) in methanol (2 ml) was added 1 ml of concentrated HCl. The suspension was cooled to 0° C. Then SnCl2 (0.094 g, 0.49 mmol) was added and the reaction mixture was stirred overnight at room temperature. The mixture was then diluted with 5 ml of water, adjusted to pH 10 with 5N NaOH and extracted with ethyl acetate (10 mL×3). The combined organic layers were washed with water, dried over K2CO3 and concentrated in vacuo. The crude product was purified by reverse phase HPLC to afford Octanedioic acid hydroxyamide [4-(2-amino-phenyl)-thiazol-2-yl]-amide 16 (0.016 g, 53% yield). NMR (400 MHz, DMSO-d6 cont 5% TFA) δ (ppm) 12.13 (1H, s), 7.56 (1H, d, J=7.0 Hz), 7.40 (1H, s), 7.09 (1H, t, J=7.0 Hz), 6.83 (1H, d, J=7.0 Hz), 6.72 (1H, m), 3.75-3.39 (4H, brs), 2.44 (2H, t, J=7.3 Hz), 2.29 (2H, t, J=7.3), 1.61 (2H, m), 1.51 (2H, m), 1.30 (4H, m).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08653278B2 |
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| Quelldatensatz | uspto-grants-2014_02 |
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| ORD ID | ord-32b3aa34c9f442b7a2bcada762483e2d |
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| Quellennotiz | uspto-grants-2014_02 |
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