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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215580Generated: October 29, 2026

N,N-Diethyl-1,3-propanediamine → 1-(4-Chloropyridin-2-yl)-3-(3-diethylaminopropyl)urea

https://huagongshe.com/reaction/2215580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-Diethyl-1,3-propanediamineHCID 61011—
ReactantPhenyl (4-chloropyridin-2-yl)-N-(phenoxycarbonyl)carbamateHCID 21054897—
SolventDimethylformamideHCID 6228—
Product1-(4-Chloropyridin-2-yl)-3-(3-diethylaminopropyl)ureaHCID 2194909354.5%

Reaction Steps

Phenyl(4-chloropyridin-2-yl)-N-(phenoxycarbonyl)carbamate (738 mg, 2.00 mmol) was dissolved in N,N-dimethylformamide (8.0 ml); N,N-diethyl-1,3-diaminopropane (1.57 ml, 10.0 mmol) was added thereto; and the reaction mixture was stirred at room temperature for 1 hour. The reaction mixture was partitioned between water and ethyl acetate; and the organic layer was washed with brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (Fuji Silysia NH, hexane-ethyl acetate-methanol system) to yield the title compound (309 mg, 1.09 mmol, 54.3%) as a pale brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109219B2
Source datasetuspto-grants-2006_09
ORD IDord-b2d57b0db43d419c90334ae4babe0c6f
Source noteuspto-grants-2006_09