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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119867Generated: November 2, 2026

Methanethiol → HCID 10131763, compound

https://huagongshe.com/reaction/2119867

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanethiolHCID 878—
ReactantSodium MethoxideHCID 10942334—
ReactantHCID 69878366HCID 69878366—
SolventMethanolHCID 887—
ProductHCID 10131763HCID 10131763—

Reaction Steps

2-Chloromethyl-1-phenylmethyl-1H-imidazo-[4,5-c]quinolin-4-amine hydrochloride (Example 28, prepared from 2.11 g of the alcohol) was added to a solution of methanethiol (1.33 g; 0.028 mol) and sodium methoxide (1.5 g; 0.028 mol) in methanol. The solid dissolved upon addition and a cream colored solid precipitated during addition. After stirring at room temperature for several hours the mixture was diluted with water. The solid was filtered from the mixture, washed with water, and dried. A crude yield of 2.3 g was obtained. The product was purified by silica gel flash chromatography (10% methanol in ethyl acetate eluent) and recrystallized from methanol/dichloromethane to give a cream colored solid, m.p. 217-219° C. Analysis: Calculated: C, 68.2; H, 5.4; N, 16.8. Found: C, 67.5; H, 5.3; N, 16.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06686472B2
Source datasetuspto-grants-2004_02
ORD IDord-12d11f7574af4f10a3ee2f987b2c683d
Source noteuspto-grants-2004_02