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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507378Generated: October 31, 2026

Hydrochloric Acid → HCID 67974881, compound

https://huagongshe.com/reaction/1507378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantSimtuzumabHCID 17750227—
ReactantHCID 53212388HCID 53212388—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventWaterHCID 962—
SolventDiethylene Glycol Monomethyl EtherHCID 8134—
ProductHCID 67974881HCID 6797488168.6%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 2-chloro-6-methoxy-3-(trifluoromethyl)quinoxaline (Intermediate 11, 150 mg, 0.571 mmol), 4-carboxy-2-chlorophenylboronic acid (115 mg, 0.571 mmol), K2CO3 (160 mg, 1.14 mmol) and Pd(dppf)Cl2 (50 mg, 0.0612 mmol) in diethylene glycol monomethyl ether (2 mL) and water (0.6 mL) was stirred at 120° C. under N2 atmosphere for 2 hours. The resulting mixture was cooled to room temperature and diluted with water (50 mL), acidified with aqueous HCl (2M) until pH=5, extracted with EtOAc (50 mL×3), dried over Na2SO4 and concentrated in vacuo. The residue was purified by column chromatography on silica gel (PE/EtOAc=1/1) to give the product (150 mg, yield 68%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221810B2
Source datasetuspto-grants-2015_12
ORD IDord-4032a02960f9425a8180cc0f902d5aaf
Source noteuspto-grants-2015_12