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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2366209Erstellt: 25. Oktober 2026

Hydrochloric Acid → HCID 86723308, Verbindung

https://huagongshe.com/reaction/2366209

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium hydrideHCID 24758—
Edukt2-Chloro-3-fluoropyridin-4-amineHCID 60150289—
Edukt2,6-Dichloro-4-cyanobenzoyl chlorideHCID 86648956—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 86723308HCID 8672330867%

Reaktionsschritte

2-Chloro-3-fluoropyridin-4-ylamine (146 mg, 10 mmol) was added to a suspension of sodium hydride (60% dispersed in mineral oil, 80 mg, 2.0 mmol) in DMF (5 mL). The mixture was stirred for 30 minutes then 2,6-dichloro-4-cyano-benzoyl chloride (250 mg, 1.1 mmol) was added and stirring continued for 18 hours. Water (10 mL) and DCM (20 mL) were added to the reaction, and the resultant mixture was acidified with 1M HCl. The organic phase was separated, washed with brine (10 mL), dried over MgSO4, and concentrated to dryness under reduced pressure. The residue was purified by silica gel flash chromatography eluting with DCM. The crude product was triturated with diethyl ether to give the desired compound as a white solid (230 mg, 67% yield). 1H NMR (400 MHz, CDCl3): δ 8.46 (t, J=5.3 Hz, 1H), 8.25 (d, J=5.5 Hz, 1H), 7.88 (br s, 1H), 7.72 (s, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08697708B2
Quelldatensatzuspto-grants-2014_04
ORD IDord-ec9bf64c5c4946de980881265aec6ee8
Quellennotizuspto-grants-2014_04