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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1743118Generated: November 4, 2026

N,N-Dimethyl-1,3-propanediamine → HCID 67527701, compound

https://huagongshe.com/reaction/1743118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-Dimethyl-1,3-propanediamineHCID 7993—
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
ReactantHCID 67527329HCID 67527329—
SolventPyridineHCID 1049—
ProductHCID 67527701HCID 6752770178.2%

Reaction Steps

A pyridine (120 mL) solution of 2-(2-diethylamino-5-aminopyrimidin-4-ylamino)-3-(4-dimethylcarbamoyloxy-phenyl)propionic acid t-butyl ester(32.0 g, 0.067 mol) was cooled to −20° C. with a dry ice/CH3CN bath. The mixture stirred for 30 minutes, and then p-fluorobenzenesulfonyl chloride (13.18 g, 0.067 mol) was added slowly. The reaction was stirred at −20° C. for 4.5 hrs, and then 3-dimethylaminopropyl amine (8.52 mL, 0.067 mol) was added, and then the mixture was allowed to warm to room temperature overnight. The reaction was concentrated in vacuo. The residue was taken up in EtOAc (1 L), and the organic phase was washed with 0.5 M citric acid (3×900 mL), water (1×900 mL), sat. NaHCO3 (3×900 mL), brine (1×900 mL), dried (MgSO4), filtered, and concentrated in vacuo to yield a brown residue. The residue was purified by flash chromatography (50% EtOAc/hexanes on silica gel) to yield 33.04 g (77%) the title compound as a yellow foam. Rf=0.54 (3:2 EtOAc/hexanes on silica gel).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07008949B2
Source datasetuspto-grants-2006_03
ORD IDord-020f80a4b1a7452eb93fc3305d9083dc
Source noteuspto-grants-2006_03