HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1949150Erstellt: 26. Oktober 2026
Hexane → 2-chloro-N-(thiophen-2-ylmethyl)quinoline-3-carboxamide
https://huagongshe.com/reaction/1949150
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Hexane | HCID 8058 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | (2-Thienylmethyl)amine | HCID 34005 | — |
| Edukt | 2-Chloroquinoline-3-carboxylic acid | HCID 847163 | — |
| Lösungsmittel | Thionyl Chloride | HCID 24386 | — |
| Produkt | 2-chloro-N-(thiophen-2-ylmethyl)quinoline-3-carboxamide | HCID 86645338 | 48% |
Reaktionsschritte
A solution of 2.1 g (10.0 mmol) 2-chloroquinoline-3-carboxylic acid in thionyl chloride (60 ml) was heated for 2 h at 85° C. Then excess thionyl chloride was removed under vacuum. The residue was taken up with DCM (60 ml) and the solution was cooled to 0° C. and then mixed with 4.0 ml (30.0 mmol) NEt3 and 1.03 ml (10.0 mmol) thiophene-2-methylamine. After stirring for 90 min at RT it was diluted with EE and washed with a saturated aqueous NH4Cl solution. The aqueous phase was extracted with EE. The combined organic phases were washed with brine, dried over Na2SO4, filtered and concentrated to small volume under vacuum. Column chromatography (hexane/EE 4:1) with the residue yielded 1.44 g (4.8 mmol, 48%) 2-chloro-N-(thiophen-2-ylmethyl)quinoline-3-carboxamide.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08399673B2 |
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| Quelldatensatz | uspto-grants-2013_03 |
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| ORD ID | ord-86a2f937289f468ba8a929400e90d358 |
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| Quellennotiz | uspto-grants-2013_03 |
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