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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816021Generated: October 29, 2026

2-Aminopyridine → N-(2-pyridyl)-4-chlorophthalimide

https://huagongshe.com/reaction/1816021

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminopyridineHCID 10439—
ReactantHCID 54187688HCID 54187688—
Solvent1,2,3-TrichlorobenzeneHCID 6895—
ProductN-(2-pyridyl)-4-chlorophthalimideHCID 432950584%

Reaction Steps

5.2 grams of 4-chlorotetrahydrophthalic anhydride, 2.6 grams of 2-aminopyridine, 50 milliliters of trichlorobenzene and 6.0 grams of Calgon Carbon S-Sorb was combined in a 3 neck flask. The flask was fitted with a reflux condenser and an inlet tube adjusted to deliver air as bubbles below the surface. The third neck was fitted with a drying tube to remove water. After about 9 hours, N-(2-pyridyl)-4-chlorophthalimide was formed in about 84% yield as determined by GC-MS.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06881815B2
Source datasetuspto-grants-2005_04
ORD IDord-94035aa56f0d423395ae981a716e2d53
Source noteuspto-grants-2005_04