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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445216Generated: November 2, 2026

Trifluoroacetic acid → HCID 178510389, compound

https://huagongshe.com/reaction/1445216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 56833954HCID 56833954—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 178510389HCID 17851038980%

Reaction Steps

To a solution of 4-cyano-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carboxylic acid {2-cyclohex-1-enyl-4-[1-(2-morpholin-4-yl-ethyl)-piperidin-4-yl]-phenyl}-amide (650 mg, 1.05 mmol) (as prepared in the previous step) in 10 mL of DCM was added 0.3 mL of EtOH and 3.0 mL of TFA, and the reaction was allowed to proceed for 2 h at 25° C. The reaction was diluted with 10 mL of EtOH and concentrated. The title compound was purified by RP-HPLC (C18), eluting with 30-50% CH3CN in 0.1% TFA/H2O over 9 min to give 600 mg (80%) of a white solid. 1H-NMR (400 MHz, CD3ID): δ 8.18 (d, 1H), 8.04 (s, 1H), 7.24 (dd, 1H), 7.14 (d, 1H), 5.84 (m, 1H), 3.84 (m, 4H), 3.76 (m, 2H), 3.50 (m, 2H), 3.30-3.10 (m, 4H), 2.92 (m, 5H), 2.30 (m, 4H), 2.20-2.00 (m, 4H), 1.90-1.74 (m, 4H). Mass spectrum (ESI, m/z): Calcd. for C28H36N6O2, 489.2, found 489.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662837B2
Source datasetuspto-grants-2010_02
ORD IDord-0159a5450d4c476299768db66e6ac395
Source noteuspto-grants-2010_02