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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1469161Generated: October 31, 2026

Trifluoroacetic acid → HCID 178463297, compound

https://huagongshe.com/reaction/1469161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 178463298HCID 178463298—
SolventDichloromethaneHCID 6344—
ProductHCID 178463297HCID 17846329799%

Reaction Steps

To a stirred solution of tert-butyl((trans)-4-((3-(((4,6-dimethyl-2-oxo-1,2-dihydro pyridin-3-yl)methyl)carbamoyl)-2-methyl-5-(3-morpholinoprop-1-yn-1-yl)phenyl)(ethyl)amino)cyclohexyl)(methyl)carbamate (1 equiv.) in DCM at 0° C., TFA (3 equiv.) was added and reaction was stirred for 2 h at room temperature. After completion, reaction was concentrated to dryness. The residue was then basified with Na2CO3 (aq.) to pH 8 and the aqueous layer was extracted with 20% methanol in DCM. The combined organic layers were dried over Na2SO4 and solvent was removed under reduced pressure to afford the title compound (99% yield) which was used in the next reaction without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006242B2
Source datasetuspto-grants-2015_04
ORD IDord-af4fbf18603744689a860cef02efe685
Source noteuspto-grants-2015_04