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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 63036Erstellt: 24. Oktober 2026

Diisopropylethylamine → 3-[(4-Cyanobenzyl)amino]pyridine-4-carboxylic acid

https://huagongshe.com/de/reaction/63036

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt3-Fluoropyridine-4-carboxylic acidHCID 345361—
Edukt4-(Aminomethyl)benzonitrile hydrochlorideHCID 9942250—
LösungsmittelDimethylacetamideHCID 31374—
Produkt3-[(4-Cyanobenzyl)amino]pyridine-4-carboxylic acidHCID 8672819518%

Reaktionsbedingungen

Temperatur166 °C

Reaktionsschritte

3-Fluoroisonicotinic acid (100 mg, 0.71 mmol), 4-(aminomethyl)-benzonitrile hydrochloride (240 mg, 1.42 mmol), and DIEA (250 μL, 1.42 mmol) were combined in DMA (2 mL) and the reaction mixture was stirred at 166° C. in a microwave for 90 min. The solution was concentrated in vacuo and purified by silica gel chromatography (10-20% MeOH/DCM). The semi-pure fractions were concentrated and then taken up in water to give a pale yellow precipitate, which was collected by filtration and dried under vacuum to give 32 mg (18%) of the title compound. 1H NMR (500 MHz, DMSO-d6): δ 8.10 (br s, 1H), 8.04 (s, 1H), 7.83 (d, 1H, J=5.0 Hz), 7.81 (d, 2H, J=8.0 Hz), 7.58 (d, 1H, J=5.0 Hz), 7.54 (d, 2H, J=8.0 Hz), 4.69 (s, 2H). [M+H] calc'd for C14H11N3O2, 254. found 254.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09447045B2
Quelldatensatzuspto-grants-2016_09
ORD IDord-0d745710e5544d009a976982d437d216
Quellennotizuspto-grants-2016_09