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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415562Generated: October 29, 2026

Methyl iodide → HCID 66619845, compound

https://huagongshe.com/reaction/415562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 86633747HCID 86633747—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 66619845HCID 66619845—

Reaction Steps

tert-Butyl 2-(2-thioxo-2,3-dihydro-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl)ethylcarbamate (31 g, 89.8 mmol) in water (150 mL) and ethanol (150 mL) was treated with ammonium hydroxide (30 mL) and iodomethane (25.5 g, 180 mmol) according to the general method of Part E of Example 22. After three hours, most of the ethanol was removed under reduced pressure, and water (500 mL) was added to the resulting suspension. The mixture was allowed to stand for 30 minutes. A solid was present and was isolated by filtration, washed with water and diethyl ether, and dried under vacuum for three hours to provide tert-butyl 2-[2-(methylthio)-1H-imidazo[4,5-c][1,5]naphthyridin-1-yl]ethylcarbamate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088788B2
Source datasetuspto-grants-2012_01
ORD IDord-4ed034f4c1ef4bdfad41ed97e7082cb0
Source noteuspto-grants-2012_01