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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 602294Generated: October 30, 2026

Cyanogen Bromide → HCID 59510519, compound

https://huagongshe.com/reaction/602294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 59510469HCID 59510469—
SolventDichloromethaneHCID 6344—
ProductHCID 59510519HCID 5951051966%

Reaction Steps

To a solution of 4-amino-5-chloro-2-ethoxy-N-[{4-(4-piperidinylmethyl)-2-morpholinyl}-methyl]benzamide (Example 22) (1.0 g) and TEA (0.41 ml) in methylene chloride (10 ml) was added cyanogen bromide (0.27 g) at room temperature, and then the mixture was stirred for 4 hours, washed with water, then brine and dried over anhydrous magnesium sulfate. Then, the solvent was removed in vacuo. The residue was purified by silica gel column chromatography (eluent: chloroform/methanol=10/1) to give the titled compound (0.7 g) as a white solid. Melting point 197° C. (degradation, recrystallized from E)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906510B2
Source datasetuspto-grants-2011_03
ORD IDord-5484bf5c39ad4bf295ea49a01cdee019
Source noteuspto-grants-2011_03