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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 445103Generated: October 29, 2026

Triethylamine → HCID 16051381, compound

https://huagongshe.com/reaction/445103

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantButyl chloroformateHCID 61140—
ReactantHCID 9843452HCID 9843452—
SolventDichloromethaneHCID 6344—
ProductHCID 16051381HCID 1605138167.2%

Reaction Steps

Triethylamine (2.67 mL, 5 eq) was added to a chilled (ice/water bath) suspension of N-{2-[4-amino-2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl]-1,1-dimethylethyl}methanesulfonamide (1.5 g, 1 eq) in dichloromethane (150 mL). A solution of butyl chloroformate (1.73 g, 3.3 eq) in dichloromethane (5 mL) was added dropwise to give a clear solution. The reaction mixture was allowed to come to ambient temperature with stirring for 24 hours. The reaction mixture was washed sequentially with water (150 mL), 4% sodium carbonate (150 mL), water (150 mL), and brine (150 mL). The organic layer was concentrated under reduced pressure. The residue was purified by automated flash chromatography (silica gel eluted with a linear gradient of 0-20% CMA in chloroform, 1500 mL) followed by recrystallization from diethyl ether to provide 1.23 g of propyl 2-ethoxymethyl-1-{2-methyl-2-[(methylsulfonyl)amino]propyl}-1H-imidazo[4,5-c]quinolin-4-ylcarbamate as a white powder, mp 125-127° C. Anal calcd for C23H33N5O5S: C, 56.19; H, 6.77; N, 14.25. Found: C, 56.35; H, 6.65; N, 14.24.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476292B2
Source datasetuspto-grants-2013_07
ORD IDord-5118cf7b607046119eebaa6e8ad06654
Source noteuspto-grants-2013_07