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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013022Generated: October 30, 2026

Sodium Iodide → HCID 67196837, compound

https://huagongshe.com/reaction/1013022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantSodium hydrideHCID 24758—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(3-Chloropropyl)-pyrrolidineHCID 11321028—
ReactantHCID 67197113HCID 67197113—
SolventDimethylformamideHCID 6228—
ProductHCID 67196837HCID 6719683723.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

4-(5-Styryl-3-trifluoromethylpyrazol-1-yl)phenol (0.2 mmol) was dissolved in N,N-dimethylformamide (1 mL), and 1-(3-chloropropyl)pyrrolidine (32 mg, 0.22 mmol), sodium hydride (9 mg, 60% dispersion in mineral oil, 0.22 mmol) and sodium iodide (33 mg, 0.22 mmol) were added. The reaction was heated at 70° C. overnight, then cooled to room temperature. Saturated sodium bicarbonate solution was added, and the mixture was extracted with ethyl acetate. The extracts were dried over MgSO4 and concentrated. Semi-prep LC-MS purification gave 20.8 mg of the desired product. LC-MS (C25H26F3N3O calculated 441) m/z 442 (M+H); 1H NMR (300 MHz, CDCl3) δ 7.42-7.30 (m, 7H), 7.12 (d, J=16.2 Hz, 1H), 7.00 (d, J=8.7 Hz, 2H), 6.88 (s, 1H), 6.77 (d, J=16.5 Hz, 1H), 4.10 (t, J=6 Hz, 2H), 2.93-2.86 (m, 6H), 2.21-2.12 (m, 2H), 1.94-1.90 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981896B2
Source datasetuspto-grants-2011_07
ORD IDord-066a65c08c0b4541a34d835c8f061689
Source noteuspto-grants-2011_07