HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 77380Erstellt: 23. Oktober 2026
Lithium Hydroxide → 2-(6-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-2-ethyl-4-oxoquinazolin-3(4H)-yl)acetic acid
https://huagongshe.com/de/reaction/77380
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Lithium Hydroxide | HCID 3939 | — |
| Edukt | Ethyl orthopropionate | HCID 66995 | — |
| Edukt | 2-(2-Amino-5-(1,4-diazabicyclo[3.2.2]nonan-4-yl)benzamido)acetic acid | HCID 67114714 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 2-(6-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-2-ethyl-4-oxoquinazolin-3(4H)-yl)acetic acid | HCID 69928597 | — |
Reaktionsschritte
2-(2-Amino-5-(1,4-diazabicyclo[3.2.2]nonan-4-yl)benzamido)acetic acid (85.3 mg, 0.27 mmol) (Intermediate 9A) (100 mg, 0.36 mmol) was dissolved in triethoxypropane (1 mL), and heated in the microwave at 160° C. for 10 minutes. Reaction allowed to cool to room temperature and lithium hydroxide solution added (0.5 mL, 1M in methanol) and reaction stirred overnight. Organic layer purified using a 1 g SCX cartridge, followed by preparative-HPLC. Purified sample was free-based using 500 mg SCX cartridge to afford 2-(6-(1,4-diazabicyclo[3.2.2]nonan-4-yl)-2-ethyl-4-oxoquinazolin-3(4H)-yl)acetic acid (76 mg, 0.21 mmol).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08841289B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-8084490e27de4145b90648157fce16ca |
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| Quellennotiz | uspto-grants-2014_09 |
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