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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750107Generated: October 28, 2026

Sodium Iodide → 7-(4-(4-(2-isopropoxyphenyl)-1,4-diazepan-1-yl)butoxy)quinolin-2(1H)-one

https://huagongshe.com/reaction/1750107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant7-(3-(4-(2,3-dichlorophenyl)-1,4-diazepan-1-yl)propoxy)quinolin-2(1H)-oneHCID 56598074—
Reactant1-(2-Isopropoxyphenyl)-1,4-diazepane hydrochlorideHCID 66631843—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product7-(4-(4-(2-isopropoxyphenyl)-1,4-diazepan-1-yl)butoxy)quinolin-2(1H)-oneHCID 5659901162.4%

Reaction Steps

A mixture of intermediate 15 (120 mg, 0.41 mmol) and NaI (123 mg, 0.82 mmol) in CH3CN was heated to reflux for 30 min and then cooled to rt. Intermediate 34 (111 mg, 0.41 mmol) and anhydrous K2CO3 (226 mg, 1.64 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=50:1) to give 7-(4-(4-(2-isopropoxyphenyl)-1,4-diazepan-1-yl)butoxy)quinolin-2(1H)-one (compound 18) (115 mg, 62%). 1H NMR (300 MHz, CDCl3) δ 11.68 (bs., 1H), 7.71 (d, J=9.3 Hz, 1H), 7.44 (d, J=9.3 Hz, 1H), 6.89-6.79 (m, 6H), 6.53 (d, J=9.6 Hz, 1H), 4.62-4.54 (m, 1H), 4.11-4.07 (m, 2H), 3.34-3.29 (m, 4H), 2.94-2.86 (m, 4H), 2.72-2.62 (m, 2H), 2.12-1.96 (m, 2H), 1.87-1.76 (m, 4H), 1.35 (d, J=6.0 Hz, 6H). HPLC: 99%, RT 2.434 min. MS (ESI) m/z 450.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156822B2
Source datasetuspto-grants-2015_10
ORD IDord-95d1d64a130747b7856b879c390c3564
Source noteuspto-grants-2015_10