Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428064Generated: October 29, 2026

Trifluoroacetic acid → HCID 11634981, compound

https://huagongshe.com/reaction/1428064

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 59128589HCID 59128589—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
ProductHCID 11634981HCID 1163498158%

Reaction Steps

To a solution of 4-cyano-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carboxylic acid [2-cyclohex-1-enyl-4-(1-methoxy-piperidin-4-yl)-phenyl]-amide (as prepared in previous step, 31 mg, 0.020 mmol) in DCM (0.5 mL) and EtOH (11 μL) was added TFA (0.1 mL). The resulting solution was stirred at RT for 6 h. The reaction mixture was concentrated in vacuo and the resulting residue was dried for 1 h, suspended in ether (10 mL) and sonicated for 5 min. The solid formed was collected by suction filtration to obtain the title compound (17.3 mg, 58%). 1H-NMR (DMSO; 400 MHz): δ 9.70 (s, 1H), 8.30 (s, 1H), 7.83 (d, 1H, J=8.4 Hz), 7.14 (d, 1H, J=8.4 Hz), 7.05 (s, 1H), 5.71 (br s, 1H), 3.30-3.55 (m, 5H), 2.41-2.62 (m, 2H), 2.12-2.19 (m, 4H), 1.60-1.85 (m, 8H). Mass spectrum (ESI, m/z): Calcd. for C23H27N5O2, 406.2 (M+H). found 406.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933091B2
Source datasetuspto-grants-2015_01
ORD IDord-fe47728c101b4e66997b88d211c9416b
Source noteuspto-grants-2015_01