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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264703Generated: November 3, 2026

Sodium Iodide → HCID 16660201, compound

https://huagongshe.com/reaction/2264703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium hydrideHCID 24758—
Reactant1-(3-Chloropropyl)-pyrrolidineHCID 11321028—
ReactantHCID 66593137HCID 66593137—
SolventDimethylformamideHCID 6228—
ProductHCID 16660201HCID 1666020147.4%

Reaction Conditions

Temperature70 °C

Reaction Steps

4-[2-(2-Methoxyethyl)indol-1-yl]phenol (0.39 mmol) was dissolved in N,N-dimethylformamide (4 mL), and 1-(3-chloropropyl)pyrrolidine (58 mg, 0.39 mmol), sodium hydride (19 mg, 60% dispersion in mineral oil, 0.47 mmol), and sodium iodide (59 mg, 0.39 mmol) were added. The reaction was heated at 70° C. for 1.5 hours, then carefully quenched with saturated sodium bicarbonate solution. The mixture was extracted with ethyl acetate, dried over MgSO4 and concentrated. The residue was purified by SiO2 chromatography to give 70 mg of the desired product. LC-MS (C24H30N2O2 calc'd 378) m/z 379 (M+H); 1H NMR (300 MHz, CDCl3) d 7.60-7.56 (m, 1H), 7.25-7.21 (m, 2H), 7.10-7.00 (m, 5H), 6.45 (s, 1H), 4.11 (t, J=6.3 Hz, 2H), 3.57 (t, J=7.2 Hz, 2H), 3.30 (s, 3H), 2.89 (t, J=7.2 Hz, 2H), 2.74 (t, J=7.5 Hz, 2H), 2.65 (m, 4H), 2.16-2.05 (m, 2H), 1.90-1.81 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855224B2
Source datasetuspto-grants-2010_12
ORD IDord-ba2053802a9f45cdbc84dc4996a95141
Source noteuspto-grants-2010_12