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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1470740Generated: November 1, 2026

Cyanogen Bromide → HCID 86666703, compound

https://huagongshe.com/reaction/1470740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantDiisopropylethylamineHCID 81531—
Reactant(S)-N-[1-(4-piperidin-4-yl-phenyl)ethyl]-acetamideHCID 67125412—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86666703HCID 86666703—

Reaction Steps

1.37 g (13.0 mmol) Cyanogen bromide are added to a mixture of 2.0 g (8.12 mmol) (S)—N-[1-(4-piperidin-4-yl-phenyl)-ethyl]-acetamide (V.1) and 4.86 mL (28.4 mmol) DIPEA in 15 mL THF and 15 mL dichloromethane. The mixture is stirred for 4 h at rt. After that time, the solvents are removed in vacuo. The residue is taken up in ethylacetate, the mixture is washed with water and the organic layer is concentrated. After addition of diethyl ether the precipitate is collected by filtration, followed by washing with diethylether to yield the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09006450B2
Source datasetuspto-grants-2015_04
ORD IDord-5416f3e277074a5e8a4cbe31e7ff442d
Source noteuspto-grants-2015_04