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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048976Generated: October 30, 2026

Methyl iodide → HCID 66692138, compound

https://huagongshe.com/reaction/1048976

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 66692195HCID 66692195—
ProductHCID 66692138HCID 66692138—

Reaction Steps

To a stirred solution of 5-(methyl-thio)-2-(pyridin-3-yl)-1H-benzo[d]imidazol-1-ol (0.36 g, 0.001 mol) in THF (20 ml) NaH (60% suspension in mineral oil), (0.14 g, 0.003 mol) was added. After stirring for the next 20 min at room temperature methyl iodide (0.39 g, 0.002 mol) was added drop wise. The resulting solution was continued to stir at room temperature for the next 3 h. The reaction was quenched with ice cold water and extracted with ethyl acetate (3×100 ml). The combined organic layers were washed with brine dried over Na2SO4 and concentrated under vacuum to afford to afford the crude compound which was purified by chromatography to obtain title compound 1-methoxy-5-(methyl-thio)-2-(pyridin-3-yl)-1H-benzo[ ]imidazole as a stick brown solid. 1H NMR (400 MHz, DMSO-d6), δ 9.47 (s, 1H), 8.74-8.73 (m, 1H), 8.53-8.50 (m, 1H), 7.71 (s, 1H), 7.49-7.33 (m, 3H), 4.05 (s, 3H) 2.58 (s, 3H). MS (M+1): 272.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382226B2
Source datasetuspto-grants-2016_07
ORD IDord-16fd269d4f65487a9793df26fe47183b
Source noteuspto-grants-2016_07