HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1161731Erstellt: 25. Oktober 2026
Sodium Bicarbonate → 2-Amino-4-(4-benzyloxy-2-methyl-phenyl)-thieno[2,3-d]pyrimidine-6-carboxylic acid ethyl ester
https://huagongshe.com/reaction/1161731
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 4-Benzyloxy-2-methylphenylboronic acid | HCID 2773245 | — |
| Edukt | Ethyl 2-amino-4-chlorothieno(2,3-d)pyrimidine-6-carboxylate | HCID 16096301 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 2-Amino-4-(4-benzyloxy-2-methyl-phenyl)-thieno[2,3-d]pyrimidine-6-carboxylic acid ethyl ester | HCID 11200943 | 71% |
Reaktionsschritte
2-methyl-4-benzyloxyphenylboronic acid (225 mg; 0.93 mmol) was added to 2-Amino-4-chloro-thieno[2,3-d]pyrimidine-6-carboxylic acid ethyl ester (example 1; step 1) (200 mg; 0.776 mmol) in DMF (10 mL). NaHCO3 (1.0M aq. Solution; 2.33 mL) was added and mixture degassed with N2. Pd(PPh3)2Cl2 was added and reaction mixture heated at 80 degrees C. for 5 hours Reaction mixture was allowed to cool to room temperature and DMF removed in vacuo. The residue was partitioned between ethyl acetate (50 mL) and sat. NaCl (aq) (50 mL) Organic phase was dried over Na2SO4 and filtered, filtrate solvents removed in vacuo to afford a yellow oil which was purified by ion-exchange chromatography (IST SCX-2 column) to afford product as a brown-yellow solid (230 mg; 71%)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07820658B2 |
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| Quelldatensatz | uspto-grants-2010_10 |
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| ORD ID | ord-3e6731320f7e48c19f5587eaabd46a8b |
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| Quellennotiz | uspto-grants-2010_10 |
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