Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1930099Generated: November 2, 2026

Propyl chloroformate → HCID 16224285, compound

https://huagongshe.com/reaction/1930099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPropyl chloroformateHCID 7998—
ReactantTriethylamineHCID 8471—
ReactantCPG-52852HCID 10309114—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 16224285HCID 1622428534.5%

Reaction Steps

Triethylamine (1.93 mL, 5 eq) was added to a chilled (ice/water bath) suspension of N-[4-(4-amino-2-ethyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]methanesulfonamide (1.0 g, 1 eq) in NMP (6.0 mL). Propyl chloroformate (1.02 g, 3 eq) was added dropwise. The reaction mixture was allowed to come to ambient temperature and stirred for 24 hours. The reaction mixture was diluted with cold water (25 mL) and then extracted with dichloromethane (50 mL). The organic layer was washed sequentially with water (2×50 mL), 4% sodium carbonate (50 mL), water (50 mL), and brine (50 mL) and then concentrated under reduced pressure. The residue was purified by automated flash chromatography (silica gel eluted with a linear gradient of 0-25% CMA in chloroform, 2000 mL) followed by recrystallization from acetonitrile to provide 0.427 g of propyl 2-ethyl-1-{4-[(methylsulfonyl)amino]butyl}-1H-imidazo[4,5-c]quinolin-4-ylcarbamate as a white solid, mp 155-157° C. Anal calcd for C21H29N5O4S: C, 56.36; H, 6.53; N, 15.65. Found: C, 56.37; H, 6.37; N, 15.70.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188111B2
Source datasetuspto-grants-2012_05
ORD IDord-2cf2ee8d8f94436fa8d7c74a71033b7f
Source noteuspto-grants-2012_05