HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 78779Erstellt: 23. Oktober 2026
2-Chloro-4-iodoaniline → 3-[(2-Chloro-4-iodophenyl)amino]isonicotinic acid
https://huagongshe.com/de/reaction/78779
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-Chloro-4-iodoaniline | HCID 282930 | — |
| Edukt | 3-Fluoropyridine-4-carboxylic acid | HCID 345361 | — |
| Edukt | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 3-[(2-Chloro-4-iodophenyl)amino]isonicotinic acid | HCID 57649651 | — |
Reaktionsschritte
To suspension of 3-fluoroisonicotinic acid (2.00 g, 14.17 mmol, in tetrahydrofuran (50 ml) at −78° C. was added lithium bis(trimethylsilyl)amide (14.3 ml, 17.01 mmol). The dark colored suspension was stirred for 15 min. In another flask, to a solution of 2-chloro-4-iodoaniline (4.7 g, 18.43 mmol) in THF (50 ml) was added lithium bis(trimethylsilyl)amide (24.9 ml, 29.77 mmol) at −78° C. under N2. The resulting green colored solution was stirred for 15 min. To this green colored solution the lithiated acid solution was added. The cold bath was removed, allowed to warm to room temperature, and stirred overnight. The mixture was filtered, and the crude was diluted with EtOAc (400 ml). It was then washed with dilute HCl (25 ml), H2O (25 ml), and dried. During concentration of the solvent, 3-[(2-chloro-4-iodophenyl)amino]isonicotinic acid was separated out as an yellow solid. (1.3 g, 24%)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08841459B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-23b0b8c07ba843b6af0aaf18ece7b1a3 |
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| Quellennotiz | uspto-grants-2014_09 |
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