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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992015Generated: October 29, 2026

Trifluoroacetic acid → HCID 11699803, compound

https://huagongshe.com/reaction/1992015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 56833953HCID 56833953—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 11699803HCID 1169980329%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of {2-[4-(4-{[4-cyano-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carbonyl]-amino}-3-cyclohex-1-enyl-phenyl)-piperidin-1-yl]-1,1-dimethyl-2-oxo-ethyl}-carbamic acid tert-butyl ester (40 mg, 0.050 mmol) in 2 mL of DCM and 20 μL of EtOH was added 1.5 mL of TFA. The solution was stirred for 3 h at 25° C., diluted with 2 mL of EtOH and concentrated in vacuo. Trituration of the residue with ether afforded 8.4 mg (29%) of the title compound as a white solid. 1H-NMR (CD3OD; 400 MHz): δ 8.10 (d, 1H, J=8.4 Hz), 8.00 (s, 1H), 7.16 (d, 1H, J=8.4 Hz), 7.07 (s, 1H), 5.79 (s, 1H), 4.55-4.48 (m, 1H), 3.30 (s, 6H), 2.89-2.87 (m, 2H), 2.40-2.25 (m, 4H), 1.96-1.93 (m, 2H), 1.86-1.83 (m, 6H), 1.64-1.61 (m, 2H). Mass Spectrum (ESI, m/z): Calcd. for C26H33N6O2, 461.2 (M+H), found 461.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645755B2
Source datasetuspto-grants-2010_01
ORD IDord-72fe2fb149014fefb69f30fd6dd9ee82
Source noteuspto-grants-2010_01