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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530405Generated: November 3, 2026

Hydrochloric Acid → HCID 73297228, compound

https://huagongshe.com/reaction/530405

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 90041495HCID 90041495—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 73297228HCID 73297228—

Reaction Conditions

Temperature110 °C

Reaction Steps

A suspension of methyl 3′-methyl-5′-{[4-(trifluoromethyl)pyrimidin-2-yl]amino}biphenyl-3-carboxylate (550 mg, 1.420 mmol) and aqueous sodium hydroxide (1 M, 1.63 mL, 1.63 mmol) in methanol (9 mL) was heated to 110° C. for 10 minutes in a microwave reactor. The reaction mixture was then diluted with aqueous hydrochloric acid (2 M, 0.89 mL, 1.78 mmol), brine (20 mL), and ethyl acetate (50 mL). The layers were separated and the aqueous layer was extracted with ethyl acetate (15 mL). The combined organic layers were washed with brine (20 mL), dried over sodium sulfate, filtered, and concentrated under reduced pressure to yield 3′-methyl-5′-{[4-(trifluoromethyl)pyrimidin-2-yl]amino}biphenyl-3-carboxylic acid. MS ESI calc'd. for C19H15F3N3O2 [M+H]+ 374, found 374.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353066B2
Source datasetuspto-grants-2016_05
ORD IDord-1cd0ede9a3e641a5ba7ea8512d62b0d6
Source noteuspto-grants-2016_05