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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748385Generated: October 30, 2026

Methyl iodide → HCID 86301332, compound

https://huagongshe.com/reaction/1748385

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantHCID 86301179HCID 86301179—
SolventDimethylformamideHCID 6228—
ProductHCID 86301332HCID 8630133261%

Reaction Steps

To a cooled solution of NaH (60% in mineral oil, 12 mg, 0.3 mmol) in DMF (0.5 mL) under an atmosphere of nitrogen, was added a solution of (7-((3-chlorobenzyl)oxy)quinolin-3-yl)methanol (Example 35, 30 mg, 0.10 mmol) in DMF (0.5 mL). The reaction was stirred for 10 minutes. Methyl iodide (0.019 mL, 0.3 mmol) was added and the reaction was stirred for an additional 25 minutes at 0° C. before being quenched with a sat. NH4Cl (aq.) solution. The aqueous layer was extracted with EtOAc. The organic layers were combined and concentrated onto silica. Purification (FCC, SiO2, 0-60%, EtOAc/hexanes) afforded the title compound as a white solid (19 mg, 61%). 1H NMR (400 MHz, CDCl3) δ 8.81 (d, J=2.0 Hz, 1H), 8.05 (d, J=1.6 Hz, 1H), 7.73 (d, J=8.6 Hz, 1H), 7.50 (s, 1H), 7.46 (d, J=2.7 Hz, 1H), 7.39-7.27 (m, 4H), 5.19 (s, 2H), 4.62 (s, 2H), 3.45 (s, 3H). [M+H]=314.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150572B2
Source datasetuspto-grants-2015_10
ORD IDord-aa0ea95c8c244af890c1c2ce5c8f0bf1
Source noteuspto-grants-2015_10