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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 595409Erstellt: 25. Oktober 2026

Iodine → Ethyl 2-(6-chloro-4-(isopropylamino)pyridin-3-yl)-5-methyloxazole-4-carboxylate

https://huagongshe.com/reaction/595409

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIodineHCID 807—
EduktTriethylamineHCID 8471—
EduktTriphenylphosphineHCID 11776—
EduktEthyl 2-(6-chloro-4-(isopropylamino)nicotinamido)-3-oxobutanoateHCID 89689546—
LösungsmittelDichloromethaneHCID 6344—
ProduktEthyl 2-(6-chloro-4-(isopropylamino)pyridin-3-yl)-5-methyloxazole-4-carboxylateHCID 89689612—

Reaktionsschritte

To a stirred solution of ethyl 2-(6-chloro-4-(isopropylamino)nicotinamido)-3-oxobutanoate (27a) (200 mg, 0.58 mmol) in DCM (10 mL), triphenyl phosphine (2 equiv.), iodine (2 equiv.) and triethyl amine (3 equiv.) were added and stirred at room temperature for 4 h. The reaction mixture was diluted using DCM and washed with water. The organic layer was collected, dried over Na2SO4, filtered and concentrated. The crude material obtained was purified by column chromatography using silica gel and EtOAc: Pet. Ether as eluent to obtain the title compound, ethyl 2-(6-chloro-4-(isopropylamino)pyridin-3-yl)-5-methyloxazole-4-carboxylate. 1H NMR: 400 MHz, DMSO-d6: δ 1.25 (d, J=6.40 Hz, 6H), 1.33 (t, J=7.20 Hz, 3H), 2.67 (s, 3H), 3.90-3.95 (m, 1H), 4.31 (q, J=7.20 Hz, 2H), 6.89 (s, 1H), 8.47 (d, J=7.60 Hz, 1H), 8.54 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09242975B2
Quelldatensatzuspto-grants-2016_01
ORD IDord-10576f45f831492fb70abda062a8cd3c
Quellennotizuspto-grants-2016_01