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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 451436Generated: October 30, 2026

Cyanogen Bromide → HCID 86656706, compound

https://huagongshe.com/reaction/451436

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantSodium BicarbonateHCID 516892—
Reactant(4-Benzyl-6-methyl-pyrimidin-2-yl)-piperidin-4-yl-amine hydrochlorideHCID 67344140—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 86656706HCID 86656706—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (4-benzyl-6-methyl-pyrimidin-2-yl)-piperidin-4-yl-amine hydrochloride (255 mg, 0.8 mmol) in CH2Cl2 (1.5 mL) was added at 0° C. a suspension of sodium hydrogencarbonate (202 mg, 2.49 mmol) in water (0.5 mL) and then within 1 minute a solution of bromocyan (106 mg, 0.97 mmol) in CH2Cl2 (1 mL). The reaction was stirred at 0° C. for 45 minutes and then at room temperature over night. The reaction was diluted with CH2Cl2, washed with saturated aqueous NaHCO3 solution and with saturated aqueous NaCl solution, dried over sodium sulfate, filtered and the solvent was evaporated under reduced pressure. The residue was purified by column chromatography using a gradient from CH2Cl2 to CH2Cl2/MeOH 19:1 (v/v) as eluent. The title compound was obtained as a colorless oil (135 mg, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486967B2
Source datasetuspto-grants-2013_07
ORD IDord-ab132d7836484e4eb606e6248e0d396d
Source noteuspto-grants-2013_07