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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226112Generated: November 1, 2026

Sodium Iodide → HCID 57752713, compound

https://huagongshe.com/reaction/226112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 57752602HCID 57752602—
SolventDichloromethaneHCID 6344—
ProductHCID 57752713HCID 5775271346%

Reaction Steps

1-{3-[8-(1-Ethyl-propyl)-2,6-dimethyl-imidazo[1,2-b]pyridazin-3-yl]-2-methyl-benzofuran-7-yl}-ethanol (0.64 g, 1.63 mmol) is dissolved in CH2Cl2 (20 mL), treated with Et3N (0.27 mL, 1.95 mmol) and MsCl (0.14 mL, 1.79 mmol). The reaction is stirred at rt overnight. It is diluted with CH2Cl2 (40 mL), washed with H2O (2×40 mL); dried with Na2SO4; filtered and concentrated. The resulting crude material is dissolved in acetone (20 mL), refluxed with NaI (0.31 g, 2.04 mmol) overnight. The organic solvent is removed in vacuo, the residue is taken up with H2O (30 mL) and extracted with EtOAc (2×30 mL); the combined organic layers are dried with Na2SO4; filtered and concentrated. Purification of the crude material by chromatography gives the title compound (0.28 g, 0.75 mmol, 46%). 1H NMR (CDCl3): δ. 0.90 (t, J=7.0 Hz, 3H), 0.91 (t, J=7.0 Hz, 3H), 1.76-1.95 (m, 4H), 2.45 (s, 3H), 2.46 (s, 3H), 2.47 (s, 3H), 3.32-3.44 (m, 1H), 5.52 (dd, J=11.5, 1.3 Hz, 1H), 6.23 (dd, J=19.0, 1.3 Hz, 1H), 6.68 (s, 1H), 7.04 (dd, J=19.0, 11.5 Hz, 1H), 7.15 (d, J=1.3 Hz, 1H), 7.16 (s, 1H), 7.29 (t, J=4.8 Hz, 1H) ppm. ES-MS (m/z): calcd for C24H27N3O (M+H)+: 374.5. found: 374.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557103B2
Source datasetuspto-grants-2009_07
ORD IDord-dc63666642214bf0ada2d3dfb5eecd54
Source noteuspto-grants-2009_07