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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750103Generated: October 28, 2026

Sodium Iodide → 7-(3-(4-(2,3-dichlorophenyl)-1,4-diazepan-1-yl)propoxy)quinolin-2(1H)-one

https://huagongshe.com/reaction/1750103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant7-(3-bromopropoxy)quinolin-2(1H)-oneHCID 29975040—
ReactantUnc0006HCID 56597938—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product7-(3-(4-(2,3-dichlorophenyl)-1,4-diazepan-1-yl)propoxy)quinolin-2(1H)-oneHCID 5659807439.3%

Reaction Steps

A mixture of intermediate 32 (217 mg, 0.77 mmol) and NaI (231 mg, 1.54 mmol) in CH3CN was heated to reflux for 30 min and then cooled to rt. Intermediate 2 (217 mg, 0.77 mmol) and anhydrous K2CO3 (425 mg, 3.08 mmol) were added to the mixture. The resulting mixture was heated to reflux and stirred overnight. The reaction solution was diluted with water and extracted with EtOAc. The combined EtOAc layers were washed with brine, dried over anhydrous Na2SO4, concentrated in vacuo and purified by flash chromatography on silica gel column (elution with DCM/MeOH=30:1) to give 7-(3-(4-(2,3-dichlorophenyl)-1,4-diazepan-1-yl)propoxy)quinolin-2(1H)-one (compound 15) (135 mg, 39%). 1H NMR (300 MHz, CDCl3) δ 11.96 (bs., 1H), 7.72 (d, J=9.3 Hz, 1H) 7.45 (d, J=8.7 Hz, 1H), 7.09-7.07 (m, 2H), 7.01-6.99 (m, 1H), 6.83-6.81 (m, 2H), 6.54 (d, J=9.0 Hz, 1H), 4.15 (t, J=5.7 Hz, 2H), 3.31 (d, J=5.1 Hz, 4H), 2.92-2.96 (m, 4H), 2.76 (t, J=6.6 Hz, 2H), 2.03-1.01 (m, 4H). HPLC: 99%, RT 2.348 min. MS (ESI) m/z 446.1 [M+H]+. mp: 117-118° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156822B2
Source datasetuspto-grants-2015_10
ORD IDord-b12996cc42564bfeb8626343064d8b6e
Source noteuspto-grants-2015_10