HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1865902Erstellt: 26. Oktober 2026
Sodium Hydroxide → 1-(3-Aminobenzyl)-4-(2-furyl)-1H-pyrazolo[3,4-d]pyrimidine-6-amine
https://huagongshe.com/reaction/1865902
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Stannous chloride dihydrate | HCID 61436 | — |
| Edukt | 4-(2-Furyl)-1-(3-nitrobenzyl)-1H-pyrazolo[3,4-d]pyrimidine-6-amine | HCID 22015489 | — |
| Lösungsmittel | Hydrochloric Acid | HCID 313 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | 1-(3-Aminobenzyl)-4-(2-furyl)-1H-pyrazolo[3,4-d]pyrimidine-6-amine | HCID 22015499 | 115,9% |
Reaktionsschritte
A suspension of 4-(2-furyl)-1-(3-nitrobenzyl)-1H-pyrazolo[3,4-d]pyrimidine-6-amine (396 mg, 1.18 mmol) in EtOH (5 mL) was heated to 50° C., treated with a solution of SnCl2.2H2O (798 mg, 3.54 mmol) in conc. HCl (1.8 mL), stirred at 50° C. for 2 h then heated at 70° C. for 2 h. The reaction mixture was cooled, basified (5-M NaOH) filtered and the resulting solid suspended in MeOH, treated with HCl in dioxan (4-M, 2 mL), diluted with diethyl ether and filtered to give the title compound (419 mg, 94%) as a yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07629349B2 |
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| Quelldatensatz | uspto-grants-2009_12 |
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| ORD ID | ord-170fe3c7fd344cd7aa92e47c8794f344 |
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| Quellennotiz | uspto-grants-2009_12 |
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