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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598771Generated: October 30, 2026

Sodium Iodide → 8-Methoxy-3-methyl-1-[4-(3-pyrrolidin-1-ylpropoxy)phenyl]-4,5-dihydro-1H-benzo[g]indazole

https://huagongshe.com/reaction/598771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium hydrideHCID 24758—
Reactant1-(3-Chloropropyl)-pyrrolidineHCID 11321028—
Reactant4-(8-Methoxy-3-methyl-4,5-dihydrobenzo[g]indazol-1-yl)-phenolHCID 58948765—
SolventDimethylformamideHCID 6228—
SolventSodium BicarbonateHCID 516892—
Product8-Methoxy-3-methyl-1-[4-(3-pyrrolidin-1-ylpropoxy)phenyl]-4,5-dihydro-1H-benzo[g]indazoleHCID 2478456420.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

4-(8-Methoxy-3-methyl-4,5-dihydrobenzo[g]indazol-1-yl)-phenol (0.1 mmol) was dissolved in N,N-dimethylformamide (1 mL), and -(3-chloropropyl)pyrrolidine (15 mg, 0.1 mmol), sodium hydride (4 mg, 60% dispersion in mineral oil, 0.1 mmol) and sodium iodide (15 mg, 0.1 mmol) were added. The reaction was heated at 70° C. for 3 hours. The solution was diluted with saturated sodium bicarbonate and extracted with ethyl acetate. The extracts were dried over MgSO4 and concentrated. SiO2 chromatography with 2% triethylamine/10% methanol/ethyl acetate gave 8.6 mg of the desired product. LC-MS (C26H31N3O2 calculated 417) m/z 418 (M+H). 1H NMR (300 MHz, CDCl3) 7.41-7.36 (m, 2H), 7.17 (d, J=8.7 Hz, 1H), 6.99-6.94 (m, 2H), 6.67 (dd, J=8.7 Hz, 2.4 Hz, 1H), 6.40 (d, J=2.4 Hz, 1H), 4.07 (t, J=6.3 Hz, 2H), 3.52 (s, 3H), 2.91 (m, 2H), 2.72-2.58 (m, 8H), 2.30 (s, 3H), 2.12-2.04 (m, 2H), 1.86-1.81 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897634B2
Source datasetuspto-grants-2011_03
ORD IDord-3935c5a8fd484325b5dc8c941260477a
Source noteuspto-grants-2011_03