HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 642377Erstellt: 24. Oktober 2026
Sulfuric Acid → [(4-Acetyl-7-hydroxy-2-phenyl-thiazolo[4,5-c]pyridine-6-carbonyl)-amino]-acetic acid
https://huagongshe.com/de/reaction/642377
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | [(4-Ethynyl-7-hydroxy-2-phenyl-thiazolo[4,5-c]pyridine-6-carbonyl)-amino]-acetic acid | HCID 24757507 | — |
| Katalysator | Mercuric sulfate | HCID 24544 | — |
| Lösungsmittel | Acetone | HCID 180 | — |
| Produkt | [(4-Acetyl-7-hydroxy-2-phenyl-thiazolo[4,5-c]pyridine-6-carbonyl)-amino]-acetic acid | HCID 24757508 | 43,1% |
Reaktionsschritte
A mixture of [(4-ethynyl-7-hydroxy-2-phenyl-thiazolo[4,5-c]pyridine-6-carbonyl)-amino]-acetic acid (52 mg, 0.15 mmole), mercury sulfate (44 mg, 0.15 mmole), concentrated sulfuric acid (19 mg, 0.19 mmole) in 80% aqueous acetone (1.6 ml) was refluxed for 2 h before it was cooled to room temperature and concentrated. The residue was washed with water and filtered. The remaining solid was dissolved in 0.5 N NaOH (15 ml) and extracted with dichloromethane (2×20 ml). The remaining aqueous layer was acidified with 1N HCl (8 ml) to pH=2. The suspension was extracted with ethyl acetate (20 ml) and dichloromethane (20 ml). The organic layer was combined, concentrated and purified by column chromatography on a C18 column with a gradient of water and acetonitrile in formic acid to give the title compound as a yellow solid (24 mg): MS: (+) m/z 372.24 (M+1), MS: (−) m/z 370.27 (M−1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07696223B2 |
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| Quelldatensatz | uspto-grants-2010_04 |
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| ORD ID | ord-fcff9ae8bd1447399e97f86b7eff9179 |
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| Quellennotiz | uspto-grants-2010_04 |
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