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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1472673Erstellt: 24. Oktober 2026

Potassium Carbonate → 4-(6-Methoxyquinazolin-2-yl)benzoic acid

https://huagongshe.com/de/reaction/1472673

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
Edukt4-Carboxyphenylboronic AcidHCID 312183—
Edukt2-Chloro-6-methoxyquinazolineHCID 59254852—
KatalysatorBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
LösungsmittelWaterHCID 962—
LösungsmittelDegme H2OHCID 49835946—
Produkt4-(6-Methoxyquinazolin-2-yl)benzoic acidHCID 6797420176,2%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A mixture of 2-chloro-6-methoxyquinazoline (Intermediate 8, 200 mg, 1.03 mmol), 4-carboxyphenylboronic acid (205 mg, 1.23 mmol) and K2CO3 (370 mg, 2.68 mmol) in DEGME/H2O (7.0 mL/2.0 mL) was degassed three times under N2 atmosphere. Then PdCl2(dppf) (75 mg, 0.103 mmol) was added and the mixture was heated to 100° C. for 3 hours under N2 atmosphere. The reaction mixture was diluted with H2O (10 mL). The aqueous layer extracted with EtOAc/MeOH (v/v=10:1, 30 mL×2). Then the aqueous layer was acidified with 2M HCl to pH 6. The precipitate was collected by filtration and washed with MeOH (10 mL), dried under high vacuum to give the desired product (220 mg, yield 76%). 1H NMR (DMSO 400 MHz): δ 13.10 (brs, 1H), 9.63 (s, 1H), 8.62 (d, J=8.0 Hz, 2H), 8.10 (d, J=8.0 Hz, 2H), 8.05 (d, J=9.2 Hz, 1H), 7.70 (dd, J=9.2, 2.8 Hz, 1H), 7.60 (d, J=2.4 Hz, 1H), 3.98 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09012646B2
Quelldatensatzuspto-grants-2015_04
ORD IDord-cc1b92af3f044eb79477bac8931db4d9
Quellennotizuspto-grants-2015_04