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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 432750Generated: October 31, 2026

Water → HCID 21936590, compound

https://huagongshe.com/reaction/432750

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 21936610HCID 21936610—
SolventDichloromethaneHCID 6344—
ProductHCID 21936590HCID 21936590—

Reaction Steps

A solution of tert-butyl 2-{2-[2-(ethoxymethyl)-5-oxido-1H-imidazo[4,5-c]quinolin-1-yl]ethoxy}ethylcarbamate (16.06 g, 37.3 mmol) in 75 mL of CH2Cl2 was treated with 75 mL of concentrated NH4OH solution. The mixture was chilled in an ice water bath. To the rapidly stirred mixture was added solid p-toluenesulfonyl chloride (7.82 g, 41.0 mmol) over a 10 min period. The reaction mixture was then warmed to room temperature. After 30 min, the reaction was treated with 75 mL of CH2Cl2 and 75 mL of water and the layers were separated. The organic portion was then washed with 1% Na2CO3 solution (2×), water, brine, dried over Na2SO4, concentrated give 14.95 g of tert-butyl 2-{2-[4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]ethoxy}ethylcarbamate as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06664265B2
Source datasetuspto-grants-2003_12
ORD IDord-200276066d7741489fead2fdf3b32638
Source noteuspto-grants-2003_12