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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350022Generated: November 3, 2026

Water → HCID 21936592, compound

https://huagongshe.com/reaction/1350022

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantAmmonium HydroxideHCID 14923—
ReactantHCID 21936588HCID 21936588—
SolventDichloromethaneHCID 6344—
ProductHCID 21936592HCID 21936592—

Reaction Steps

A solution of tert-butyl 2-[2-(2-methyl-5-oxido-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamate (11.21 g, 29.0 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 (5.53 g, 29.0 mmol) over a 10 min period. The reaction mixture was then warmed to room temperature and treated with 75 mL of CH2Cl2 and 75 mL of water. The organic portion was then washed with 1% Na2CO3 solution (3×) and brine. The organic portion was dried over Na2SO4 and concentrated and triturated in ether to yield 7.13 g of tert-butyl 2-[2-(4-amino-2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)ethoxy]ethylcarbamate as a light green solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07214675B2
Source datasetuspto-grants-2007_05
ORD IDord-794b9da211ff42d0970c463758cff9a2
Source noteuspto-grants-2007_05