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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043288Generated: November 2, 2026

Triethylamine → HCID 178510398, compound

https://huagongshe.com/reaction/1043288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilyl isocyanateHCID 70696—
Reactant4-Cyano-1h-imidazole-2-carboxylic acid (2-cyclohex-1-enyl-4-piperidin-4-yl-phenyl)-amide trifluoroacetic acid saltHCID 178510383—
SolventDichloromethaneHCID 6344—
ProductHCID 178510398HCID 17851039871.7%

Reaction Conditions

Temperature25 °C

Reaction Steps

A flask was charged with 4-cyano-1H-imidazole-2-carboxylic acid (2-cyclohex-1-enyl-4-piperidin-4-yl-phenyl)-amide TFA salt (51 mg, 0.10 mmol) (as prepared in Example 14, step (b)), NEt3 (22 μL, 0.15 mmol), trimethylsilyl isocyanate (16 μL, 0.11 mmol) and 1.0 mL of DCM and stirred for 10 h at 25° C. The solvent was evaporated and the title compound was purified by RP-HPLC (C18), eluting with 35-60% CH3CN in 0.1% TFA/H2O over 11 min to give 30 mg (70%) of a white solid. 1H-NMR (400 MHz, DMSO-d6): δ 14.28 (br s, 1H), 9.76 (s, 1H), 8.34 (s, 1H), 7.84 (d, 1H), 7.18 (dd, 1H), 7.08 (d, 1H), 6.00 (br s, 2H), 5.72 (m, 1H), 4.18 (m, 2H), 2.80-2.60 (m, 3H), 2.24-2.10 (m, 4H), 1.80-1.60 (m, 6H), 1.50 (m, 2H). Mass spectrum (ESI, m/z): Calcd. for C23H26N6O, 419.2 (M+H). found 419.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557847B2
Source datasetuspto-grants-2013_10
ORD IDord-33e464da50b94f058c623ea6f20c8260
Source noteuspto-grants-2013_10