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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873747Generated: October 31, 2026

Trifluoroacetic acid → HCID 86724294, compound

https://huagongshe.com/reaction/873747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86724251HCID 86724251—
SolventDichloromethaneHCID 6344—
ProductHCID 86724294HCID 8672429441.1%

Reaction Steps

To a mixture of tert-butyl (6′-{[(5-fluoropyridin-2-yl)carbonyl]amino}dispiro[cyclopropane-1,3′-chromene-4′,4″-[1,3]oxazol]-2″-yl)carbamate (135 mg, 0.288 mmol) and CH2Cl2 (5.4 mL) was added trifluoroacetic acid (1.30 mL, 17.0 mmol) at ambient temperature. After stirring for 2 hours at the same temperature, the mixture was concentrated at reduced pressure. The residue was partitioned between CHCl3 and saturated aqueous NaHCO3. The organic layer was washed with water, dried over Na2SO4 and filtered. The filtrate was concentrated at reduced pressure, and the residue was purified with column chromatography on silica gel (CHCl3-EtOH, a linear gradient of EtOH from 0 to 20%) to afford N-(2″-aminodispiro[cyclopropane-1,3′-chromene-4′,4″-[1,3]oxazol]-6′-yl)-5-fluoropyridine-2-carboxamide (43.6 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975415B2
Source datasetuspto-grants-2015_03
ORD IDord-456d1e2917134ad0bc2ba4379f6af3e4
Source noteuspto-grants-2015_03