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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 859043Generated: October 31, 2026

Trifluoroacetic acid → HCID 10474988, compound

https://huagongshe.com/reaction/859043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58759743HCID 58759743—
SolventDichloromethaneHCID 6344—
ProductHCID 10474988HCID 10474988—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a round-bottom flask was added {2-[6-(quinolin-7-yloxy)-pyrimidin-4-yl]-5-trifluoromethyl-phenyl}-carbamic acid tert-butyl ester, (Example 162), (3.2 g, 6.6 mmol) and CH2Cl2 (100 mL). The mixture was cooled to 0° C. and trifluoroacetic acid (25 mL) was added. After stirring for 5 min at 0° C., the mixture was allowed to warm to room temperature and stirred for 1.5 h. The reaction mixture was concentrated in vacuum and diluted with CH2Cl2 (200 mL) and satd NaHCO3 (200 mL). The phases were separated and the aqueous phase was extracted with CH2Cl2 (100 mL). The combined extracts were washed with aq NaHCO3 (20% satd NaHCO3/H2O), H2O, brine and then dried over Na2SO4, filtered and concentrated onto silica gel. Purification by silica gel chromatography (gradient, 40 to 75% EtOAc/hexanes) afforded the title compound as a yellow solid. Mp: 193–194° C. MS (ESI, pos. ion) m/z: 383.2 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148221B2
Source datasetuspto-grants-2006_12
ORD IDord-5a2a70a1534f45c3a1fa58b52388c2b0
Source noteuspto-grants-2006_12