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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750087Generated: November 1, 2026

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

https://huagongshe.com/reaction/1750087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantUnc0006HCID 56597938—
Reactant7-(3-bromopropoxy)-3,4-dihydroisoquinolin-1(2H)-oneHCID 66632107—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product7-(3-(4-(2,3-dichlorophenyl)-1,4-diazepan-1-yl)propoxy)-3,4-dihydroisoquinolin-1(2H)-oneHCID 6655958771.5%

Reaction Steps

A mixture of intermediate 20 (110 mg, 0.39 mmol) and NaI (117 mg, 0.78 mmol) in CH3CN was heated to reflux for 30 min and then cooled to rt. Intermediate 2 (165 mg, 0.58 mmol) and anhydrous K2CO3 (216 mg, 1.56 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)-3,4-dihydroisoquinolin-1(2H)-one (compound 5) (125 mg, 71%). 1H NMR (300 MHz, CDCl3) δ 7.60 (d, J=2.1 Hz, 1H), 7.14-7.08 (m, 3H), 7.02-7.00 (m, 2H), 6.02 (br., 1H), 4.10 (t, J=6.3 Hz, 2H), 3.56-3.53 (m, 2H), 3.31-3.27 (m, 4H), 2.96-2.88 (m, 6H), 2.77-2.72 (m, 2H), 2.01 (m, 4H). HPLC: 99%, RT 2.578 min. MS (ESI) m/z 448.1 [M+H]+. mp: 116-117° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156822B2
Source datasetuspto-grants-2015_10
ORD IDord-a9805980f9b64f8c8167571a3d42f7bb
Source noteuspto-grants-2015_10