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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714675Generated: November 1, 2026

N-bromobutanimide → HCID 68450954, compound

https://huagongshe.com/reaction/1714675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 68439019HCID 68439019—
SolventDichloromethaneHCID 6344—
ProductHCID 68450954HCID 6845095475.9%

Reaction Steps

To a solution of 4-(1-methoxy-piperidin-4-yl)-phenylamine (as prepared above, 42 mg, 0.20 mmol) in DCM (2 mL) was added NBS (36.2 mg, 0.20 mmol) and the reaction mixture was stirred at RT for 12 h. The reaction mixture was diluted with DCM (10 mL) and washed with saturated aqueous NaHCO3 (10 mL) and water (10 mL). The organic layer was separated, dried (Na2SO4) and concentrated in vacuo to obtain 2-bromo-4-(1-methoxy-1,2,3,6-tetrahydro-pyridin-4-yl)-phenylamine (43 mg, 74.5%) which was used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795279B2
Source datasetuspto-grants-2010_09
ORD IDord-0a543b674c4c4c78bd2196ce5fb027b7
Source noteuspto-grants-2010_09