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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1055999Erstellt: 26. Oktober 2026

Diisopropylethylamine → HCID 178522455, Verbindung

https://huagongshe.com/reaction/1055999

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
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—
Edukt2-Chloroquinoline-8-carboxylic acidHCID 19026201—
Edukt3-amino-2-hydroxy-1H-pyridin-4-oneHCID 178508083—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 178522455HCID 17852245524%

Reaktionsschritte

A mixture of 2-chloroquinoline-8-carboxylic acid (0.42 g, 2.023 mmol), 3-aminopyridine-2,4-diol (Example 179b, 0.383 g, 3.03 mmol), HATU (1.154 g, 3.03 mmol), and N-ethyl-N-isopropylpropan-2-amine (1.083 ml, 6.07 mmol) in DMF (2.023 ml) was stirred at RT for 16 h. The mixture was diluted with EtOAc (200 ml), added to a separatory funnel, and washed with water (3×100 ml) before the organic layer was separated, dried over Na2SO4, and concentrated. Purification by silica gel (100% DCM to 4% MeOH/DCM) provided 2-chloro-N-(2,4-dihydroxypyridin-3-yl)quinoline-8-carboxamide (181b, 24% yield as a yellow solid). MS (ESI, pos. ion) m/z: 316.2 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09394297B2
Quelldatensatzuspto-grants-2016_07
ORD IDord-b6f71e2ccdf04bee8957551ede2078a0
Quellennotizuspto-grants-2016_07