HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2225208Erstellt: 25. Oktober 2026
Bay-H-1127 → ethyl 2-(5-(trifluoromethyl)-1H-indazol-3-ylamino)acetate
https://huagongshe.com/reaction/2225208
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Bay-H-1127 | HCID 16736 | — |
| Edukt | Ethyl oxoacetate | HCID 70211 | — |
| Edukt | Sodium cyanoborohydride | HCID 5003444 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Acetic acid methanol | HCID 10129899 | — |
| Produkt | ethyl 2-(5-(trifluoromethyl)-1H-indazol-3-ylamino)acetate | HCID 68469013 | — |
Reaktionsschritte
Preparation I6, Step 2: A solution of 5-(trifluoromethyl)-1H-indazol-3-amine (2.08 g, 10.3 mmol) in 50 mL of 1% AcOH/MeOH was charged with ethyl glyoxylate (2.05 mL of a 50% solution in toluene, 10.3 mmol; note: the commercially available material is polymeric and was heated at 100° C. for 90 min before being used immediately in this reaction) and sodium cyanoborohydride (777 mg, 12.4 mmol). The mixture was stirred for 2.5 h, quenched with sat. NaHCO3, and extracted with EtOAc (2×). The organic extracts were combined, washed with brine, dried (sodium sulfate), filtered, and concentrated in vacuo. Purification by flash chromatography provided ethyl 2-(5-(trifluoromethyl)-1H-indazol-3-ylamino)acetate (819 mg).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07378409B2 |
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| Quelldatensatz | uspto-grants-2008_05 |
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| ORD ID | ord-6ea550606c864c1a877d8a687fbdf8ce |
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| Quellennotiz | uspto-grants-2008_05 |
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