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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445244Generated: November 1, 2026

Dichloromethane → HCID 59128572, compound

https://huagongshe.com/reaction/1445244

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBroPHCID 2733179—
ReactantHCID 68451726HCID 68451726—
Reactant4-Cyano-1h-imidazole-2-carboxylic acid (2-cyclohex-1-enyl-4-piperidin-4-yl-phenyl)-amide trifluoroacetic acid saltHCID 178510383—
ProductHCID 59128572HCID 5912857255%

Reaction Steps

A mixture of 1-(2-trimethylsilanyl-ethoxymethyl)-1H-[1,2,4]-triazole-3-carboxylic acid potassium salt (as prepared above, 28 mg, 0.10 mmol), DIEA (34 μL, 0.20 mmol), 4-(4-amino-3-cyclohex-1-enyl-phenyl)-piperidine-1-carboxylic acid tert-butyl ester (as prepared in Example 14, step (b), 35.6 mg, 0.100 mmol) and PyBroP (69.9 mg, 0.150 mmol) in DCM (2 mL) was stirred at RT for 12 h. The reaction mixture was diluted with DCM (5 mL) and washed with saturated aqueous NaHCO3 (10 mL) and water (10 mL). The organic layer was separated, dried (Na2SO4) and concentrated in vacuo The product was chromatographed on silica (20-40% EtOAc/hexane) to obtain the title compound (31.9 mg, 55%). Mass psectrum (ESI, m/z): Calcd. for C31H47N5O4Si, 481.2 (M-BOC+2H), found. 481.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662837B2
Source datasetuspto-grants-2010_02
ORD IDord-98d00a3fd9ac42298caf7c54c3eecbd6
Source noteuspto-grants-2010_02