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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382969Generated: October 27, 2026

Sodium Iodide → 4-Amino-2-(2-butanon-3-yl)oxy-5-chloro-N-[2-(dimethylamino)-ethyl]benzamide

https://huagongshe.com/reaction/1382969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Butanone, 3-bromo-HCID 13142—
Reactant4-Amino-5-chloro-N-[2-(dimethylamino)ethyl]-2-hydroxybenzamideHCID 14372582—
SolventDimethylformamideHCID 6228—
Product4-Amino-2-(2-butanon-3-yl)oxy-5-chloro-N-[2-(dimethylamino)-ethyl]benzamideHCID 1437255676.6%

Reaction Steps

A solution of 4-amino-5-chloro-N-[2-(dimethylamino)ethyl]-2-hydroxybenzamide (1.90 g, 7.37 mmoles) (prepared in Example 17), potassium carbonate (3.06 g, 2.21 mmoles), sodium iodide (1.11 g, 7.37 mmoles) and 91% 3-bromo-2-butanone (1.81 g, 12 mmoles) in DMF (30 ml) was stirred for 1.5 hours. The solvent was removed in vacuo and the residue partitioned between water and methylene chloride. The aqueous phase was extracted two more times with methylene chloride. The combined extracts were dried and concentrated in vacuo. The residue was chromatographed on a silica gel column using the solvent system of methylene chloride (99.5)-methanol (0.5)-ammonia (0.2). The appropriate fractions were combined and concentrated in vacuo to give a solid. This was recrystallized from acetonitrile to give 1.85 g of the title compound as a colorless solid, mp. 124°-125°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04808624
Source datasetuspto-grants-1989_02
ORD IDord-e105ea67c5ed4fd4bed9c367cc43fef7
Source noteuspto-grants-1989_02