HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 7629Erstellt: 23. Oktober 2026
Tetrahydrofuran → 2-[7-(3-Fluoro-benzyloxy)-2-methyl-4-oxo-4H-quinazolin-3-yl]-acetamide
https://huagongshe.com/de/reaction/7629
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Edukt | HCID 21991771 | HCID 21991771 | — |
| Edukt | 4-(3-Fluoro-benzyloxy)-2-nitro-benzoic acid methyl ester | HCID 69594337 | — |
| Edukt | 4-(3-Fluorobenzyloxy)-2-nitro-benzoic acid (3-fluoro-benzyl) ester | HCID 86593646 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-[7-(3-Fluoro-benzyloxy)-2-methyl-4-oxo-4H-quinazolin-3-yl]-acetamide | HCID 10020180 | 65% |
Reaktionsschritte
4-(3-Fluoro-benzyloxy)-2-nitro-benzoic acid: A mixture of 4-(3-fluorobenzyloxy)-2-nitro-benzoic acid (3-fluoro-benzyl) ester and 4-(3-fluoro-benzyloxy)-2-nitro-benzoic acid methyl ester (14.0 g, 35.0 mmol) in THF (120 mL) and water (120 mL), containing lithium hydroxide monohydrate (2.94 g, 70.1 mmol) was stirred at rt for 48 h. Then the mixture was poured into sodium hydroxide (2 N, 50 mL) and then the mixture extracted with diethyl ether (3×150 mL). The aqueous phase was then adjusted to pH 2 with HCl. Then the mixture was poured into sodium hydroxide (2 N, 50 mL) and the aqueous phase was then adjusted to pH 5.2 with HCl then the mixture extracted with diethyl ether (3×100 mL). The combined extracts were then washed with brine (100 mL) dried and evaporated to afford title compound (6.6 g, 65%) as a light yellow solid. MS: m/e=290.0 (M−H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07087612B2 |
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| Quelldatensatz | uspto-grants-2006_08 |
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| ORD ID | ord-ad3689421b0444ecba177dceb56a6917 |
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| Quellennotiz | uspto-grants-2006_08 |
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