Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415556Generated: October 28, 2026

Methyl iodide → HCID 66620306, compound

https://huagongshe.com/reaction/415556

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 86633746HCID 86633746—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductHCID 66620306HCID 6662030666.5%

Reaction Steps

Iodomethane (0.89 mL, 14 mmol) was added to a suspension of tert-butyl 3-(7-bromo-2-thioxo-2,3-dihydro-1H-imidazo[4,5-c]quinolin-1-yl)propylcarbamate (4 g, 9 mmol) in deionized water (25 mL), ethanol (25 mL), and ammonium hydroxide (5 mL), and the reaction was stirred for two hours at room temperature and then diluted with chloroform and water. The aqueous layer was separated and extracted four times with chloroform. The combined organic fractions were dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The crude product was dried under high vacuum to provide 2.7 g of tert-butyl 3-(7-bromo-2-(methylthio)-1H-imidazo[4,5-c]quinolin-1-yl)propylcarbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088788B2
Source datasetuspto-grants-2012_01
ORD IDord-9c779d446aa145a19caeaa27a7fbb1f4
Source noteuspto-grants-2012_01