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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1955231Generated: October 31, 2026

Cyanogen Bromide → HCID 23294469, compound

https://huagongshe.com/reaction/1955231

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 23294226HCID 23294226—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
ProductHCID 23294469HCID 2329446980%

Reaction Steps

To a solution of 4-benzyl-1-[(3,4-diaminophenoxy)ethyl]piperidine (202 mg, 0.62 mmol) in MeOH (1.5 mL) was added 130 μL of 5.0 M solution of cyanogen bromide in acetonitrile. The resulting mixture was stirred at r.t. under N2 for 24 h, then evaporated, and the residue was purified by chromatography over silica gel (CHCl3 --MeOH, 4:1) to give 174 mg (80%) of the title compound as a viscous oil. 1H NMR (CDCl3): 1.35-1.46 (m, 2H), 1.50-1.67 (m, 3H), 2.04-2.12 (m, 2H), 2.539 (d, 2H, J=7), 2.773 (t, 2H, J=6), 3.00-3.03 (m, 2H), 3.50 (bs, 1H), 4.035 (t, 2H, J=6), 6.243 (dd, 1H, J=8; 3), 6.317 (d, 1H, J=3), 6.614 (d, 1H, J=8), 7.12-7.30 (m, 5H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124323
Source datasetuspto-grants-2000_09
ORD IDord-ad902e95746e46d0bcce650dbc76253e
Source noteuspto-grants-2000_09