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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1472673Generated: October 25, 2026

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

https://huagongshe.com/reaction/1472673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Carboxyphenylboronic AcidHCID 312183—
Reactant2-Chloro-6-methoxyquinazolineHCID 59254852—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
SolventDegme H2OHCID 49835946—
Product4-(6-Methoxyquinazolin-2-yl)benzoic acidHCID 6797420176.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012646B2
Source datasetuspto-grants-2015_04
ORD IDord-cc1b92af3f044eb79477bac8931db4d9
Source noteuspto-grants-2015_04