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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889184Generated: November 2, 2026

Trifluoroacetic acid → HCID 59610053, compound

https://huagongshe.com/reaction/1889184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 59610043HCID 59610043—
ProductHCID 59610053HCID 59610053—

Reaction Steps

Trifluoroacetic acid (5 ml) was added to 4-{2-[tert-Butoxycarbonyl-(4-methoxy-benzyl)-amino]-thiazol-5-yl}-benzoic acid ethyl ester (300 mg, 0.64 mmol) at room temperature and reaction mixture was refluxed for 5 hrs. Trifluoroacetic acid was removed on rotavapour. The residue was taken in water (10 ml) and ethyl acetate (15 ml) and basified this with sodium bicarbonate, layers were separated, and aq. layer was re-extracted with ethyl acetate (15 ml). The combined organic layer was washed with brine (15 ml) and dried over anhydrous sodium sulfate. Solvent was evaporated on rotavapour to get the solid product. The crude material was used for the next step with out any further purification,(150 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501955B2
Source datasetuspto-grants-2013_08
ORD IDord-90de1b3fe7384890a2ecddf97f9df9cc
Source noteuspto-grants-2013_08