HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1432263Erstellt: 25. Oktober 2026
Ammonium Chloride → (1-(4-Fluorobenzyl)-5-methanesulfonylindol-2-yl)(thiazol-2-yl)-methanol
https://huagongshe.com/reaction/1432263
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 2-Bromothiazole | HCID 76430 | — |
| Edukt | 1-(4-Fluorobenzyl)-5-methanesulfonylindole-2-carbaldehyde | HCID 22504374 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | (1-(4-Fluorobenzyl)-5-methanesulfonylindol-2-yl)(thiazol-2-yl)-methanol | HCID 22504451 | 28,6% |
Reaktionsschritte
To a mixture of 2-bromothiazole (123 mg) and tetrahydrofuran (3.5 ml), 1.61 M n-butyl lithium solution in hexane (0.51 ml) was added at −78° C. and the mixture was stirred for 30 minutes, followed by addition of a solution of 1-(4-fluorobenzyl)-5-methanesulfonylindole-2-carbaldehyde (50 mg) obtained in Example 27 (4) in tetrahydrofuran (3.5 ml) at the same temperature, and the mixture was stirred as such for 30 minutes. The reaction mixture was poured into a saturated aqueous ammonium chloride solution, extracted with chloroform, washed with water, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was subjected to silica gel preparative thin-layer chromatography (hexane:ethyl acetate=1:1) to obtain 18 mg of the desired product as a yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07612070B2 |
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| Quelldatensatz | uspto-grants-2009_11 |
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| ORD ID | ord-a1f24ac8428a4affa5a6823a6e025d62 |
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| Quellennotiz | uspto-grants-2009_11 |
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