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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043326Generated: October 31, 2026

Dichloromethane → HCID 59128572, compound

https://huagongshe.com/reaction/1043326

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 spectrum (ESI, m/z): Calcd. for C31H47N5O4Si, 481.2 (M-BOC+2H). found. 481.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557847B2
Source datasetuspto-grants-2013_10
ORD IDord-c80777318c4543e590a08a020b2101cc
Source noteuspto-grants-2013_10