HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1047413Erstellt: 26. Oktober 2026
Phenol, 4-amino-2-fluoro- → 4-[[2-[5-[[Boc(2-methoxyethyl)amino]methyl]-2-pyridyl]-7-thieno[3,2-b]pyridyl]oxy]-3-fluoroaniline
https://huagongshe.com/reaction/1047413
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phenol, 4-amino-2-fluoro- | HCID 2735918 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Edukt | tert-Butyl ((6-(7-chlorothieno[3,2-b]pyridin-2-yl)pyridin-3-yl)methyl)(2-methoxyethyl)carbamate | HCID 57919613 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 4-[[2-[5-[[Boc(2-methoxyethyl)amino]methyl]-2-pyridyl]-7-thieno[3,2-b]pyridyl]oxy]-3-fluoroaniline | HCID 57919472 | 58% |
Reaktionsschritte
To a solution of 4-amino-2-fluorophenol (4) (1.933 g, 15.21 mmol) in DMSO (30 mL) was added potassium tert-butoxide (2.017 g, 17.97 mmol). After 30 min, intermediate 11 (6 g, 13.83 mmol) was added and the reaction mixture was heated at 100° C. for 45 min. The reaction mixture was then cooled down, poured in water (250 mL) at 40-45° C. and the resultant suspension was stirred for 30 min. The precipitate was collected by filtration, washed with water (2×30 mL) and dried overnight. The dry solid was triturated with Et2O (50 mL), to afford intermediate 13 (4.18 g, 58% yield) as a brown solid. MS (m/z): 525.2 (M+H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08569503B2 |
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| Quelldatensatz | uspto-grants-2013_10 |
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| ORD ID | ord-32e26959e3a74868a7fa203d602d7127 |
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| Quellennotiz | uspto-grants-2013_10 |
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