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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547505Generated: November 1, 2026

Cyanogen Bromide → HCID 178512262, compound

https://huagongshe.com/reaction/547505

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 59738211HCID 59738211—
SolventDichloromethaneHCID 6344—
ProductHCID 178512262HCID 17851226241%

Reaction Steps

A mixture of 6-carbamimidoyl-2-(3-fluorophenethylamino)-N-(pyridin-3-ylmethyl)nicotinamide (0.013 g, 0.034 mmol), CNBr (3N, 0.017 mL, 0.051 mmol), DIPEA (0.0085 mL, 0.051 mmol), in DCM (0.10 mL) was stirred at room temperature until the reaction was complete. The reaction mixture was concentrated to dryness and purified by RP-HPLC using a mixture of acetonitrile and H2O to give 6-(N-cyanocarbamimidoyl)-2-(3-fluorophenethylamino)-N-(pyridin-3-ylmethyl)nicotinamide as a solid (0.0058 g, 41%). LC/MS (M+H+) m/z 418.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939548B2
Source datasetuspto-grants-2011_05
ORD IDord-c438e32e7fc74388b8f5caccd093611f
Source noteuspto-grants-2011_05