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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2355095Erstellt: 26. Oktober 2026

Diisopropylamine → 2-methyl-5-nitro-N-(pyrimidin-5-yl)benzamide

https://huagongshe.com/reaction/2355095

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylamineHCID 7912—
EduktPyrimidin-5-amineHCID 344373—
Edukt2-Methyl-5-nitrobenzoic acidHCID 519683—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-methyl-5-nitro-N-(pyrimidin-5-yl)benzamideHCID 24823255—

Reaktionsschritte

In a 2 L round bottom flask with mechanical stirring was charged with 2-methyl-5-nitrobenzoic acid (20 g), HATU (38 g) and diisopropylamine (32 mL) in DMF (90 mL). This mixture was stirred for 30 min then pyrimidin-5-amine was added and the reaction was stirred for 18 hr. The LCMS showed complete conversion. DMF was removed under vacuum as much as possible then water was added and a solid precipitated out (use mechanical stirring). The tan solid was filtered and rinsed with water, then taken up in EtOAc, washed with brine, dried over MgSO4, filtered and concentrated down. The crude was taken up in EtOAc and the product 45 precipitated out. This was filtered and the filtrate was concentrated down and taken up in EtOAc/Hex. After standing overnight, more solids were filtered and were combined with the first crop. 2-methyl-5-nitro-N-(pyrimidin-5-yl)benzamide 45 was obtained as a light yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07754717B2
Quelldatensatzuspto-grants-2010_07
ORD IDord-5d7b5c1d48794e1cb5ccdf93ebef697c
Quellennotizuspto-grants-2010_07