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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1811744Generated: November 1, 2026

Trifluoroacetic acid → HCID 59224712, compound

https://huagongshe.com/reaction/1811744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 59224709HCID 59224709—
SolventDichloromethaneHCID 6344—
ProductHCID 59224712HCID 59224712108.3%

Reaction Steps

5-[2-Amino-6-(2-tert-butoxycarbonylaminoethylsulfanyl)pyrimidin-4-yl]-2,4-dimethylbenzoic acid methyl ester (531 mg, 1.23 mmol) obtained in Step 1 above was dissolved in dichloromethane (3.0 ml). Trifluoroacetic acid (1.5 ml) was added to the solution, and stirred at room temperature for 1 hour. The reaction solution was concentrated under reduced pressure. The resulting residue was diluted with ethyl acetate, and then a saturated aqueous sodium bicarbonate solution was added thereto. The organic layer was separated, and the aqueous layer was extracted with ethyl acetate. The organic layers were combined together, and sequentially washed with water and a saturated aqueous sodium chloride solution. The ethyl acetate solution was dried over anhydrous magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure to yield the crude product of 5-[2-amino-6-(2-aminoethylsulfanyl)pyrimidin-4-yl]-2,4-dimethylbenzoic acid methyl ester (443 mg) as a white solid material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362236B2
Source datasetuspto-grants-2013_01
ORD IDord-22b74e1ad7fc4ea98b684bb35530ea18
Source noteuspto-grants-2013_01