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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597314Generated: October 31, 2026

Trimethylsilyl isocyanate → HCID 17808983, compound

https://huagongshe.com/reaction/1597314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl isocyanateHCID 70696—
ReactantHCID 10937790HCID 10937790—
SolventDichloromethaneHCID 6344—
ProductHCID 17808983HCID 1780898366.4%

Reaction Steps

To a solution of 4-amino-5-chloro-2-methoxy-N-[1-(4-piperidinylmethyl)-4-piperidinyl]benzamide (610 mg) in methylene chloride (30 ml) is added trimethylsilyl isocyanate (180 mg) under ice-cooling, and the mixture is stirred at room temperature for 15 hours. The reaction mixture is washed with water and a saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and the solvent is evaporated under reduced pressure. The residue is purified by basic silica gel column chromatography (eluent; chloroform: methanol=40:1) to give 4-amino-5-chloro-N-[1-(1-carbamoyl-4-piperidinylmethyl)-4-piperidinyl]-2-methoxybenzamide (440 mg) as white amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06294555B1
Source datasetuspto-grants-2001_09
ORD IDord-e1055962f6134a47b7b86f6b8f234d89
Source noteuspto-grants-2001_09