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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 14297Erstellt: 26. Oktober 2026

N-Methylbutylamine → Methyl 3-{[butyl(methyl)amino]carbonyl)-5-iodobenzoate

https://huagongshe.com/reaction/14297

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-MethylbutylamineHCID 8068—
EduktDiisopropylethylamineHCID 81531—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Edukt3-Iodo-5-(methoxycarbonyl)benzoic acidHCID 15840391—
LösungsmittelDimethylformamideHCID 6228—
ProduktMethyl 3-{[butyl(methyl)amino]carbonyl)-5-iodobenzoateHCID 21086165—

Reaktionsschritte

3-Iodo-5-(methoxycarbonyl)benzoic acid (1 g, 3.3 mmol) is dissolved in DMF (10 mL), and diisopropylethylamine (1.7 mL, 9.8 mmol), HATU (1.5 g, 3.9 mmol), and N-methylbutylamine (581 μL, 4.9 mmol) are added. The reaction stirred at room temperature 2 h. The reaction is partitioned between ethyl acetate and water. The organic layer is washed with saturated sodium bicarbonate, and saturated sodium chloride, dried (sodium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 40% ethyl acetate/hexane) provides the title compound. ESI MS m/z 376.1 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07727997B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-8da84dc1edd148bab8666c6537bcb486
Quellennotizuspto-grants-2010_06