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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2308984Generated: October 25, 2026

N-3-Bromopropylphthalimide → N-[3-(N-phenyl-N-pyrid-2-ylamino)propyl]phthalimide

https://huagongshe.com/reaction/2308984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-3-BromopropylphthalimideHCID 21611—
ReactantSodium hydrideHCID 24758—
ReactantN-2-PyridylanilineHCID 81130—
ReactantHCID 178418361HCID 178418361—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductN-[3-(N-phenyl-N-pyrid-2-ylamino)propyl]phthalimideHCID 20186606—

Reaction Conditions

Temperature85 °C

Reaction Steps

A solution of 2-(N-phenylamino)pyridine (5.0 g) in DMSO (15 ml) was added to a suspension of sodium hydride (0.78 g) in DMSO (20 ml). The mixture was stirred and slowly heated under nitrogen to 85° C. After the evolution of hydrogen had ceased, the mixture was cooled to room temperature and a solution of N-(3-bromopropyl)phthalimide (7.88 g) in DMSO (15 ml) added dropwise. The mixture was allowed to stand overnight and then poured into water. The aqueous phase was made acid to a pH between 2 to 4 and extracted with ether. The extracts were dried (MgSO4), the ether evaporated and the residue crystallised from ethanol to give N-[3-(N-phenyl-N-pyrid-2-ylamino)propyl]phthalimide, 3.69 g (35%) m.p. 103°-105° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04692456
Source datasetuspto-grants-1987_09
ORD IDord-ef1965a29c304b348a573de56f31640e
Source noteuspto-grants-1987_09