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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 514599Generated: October 28, 2026

Triethylamine → HCID 66765490, compound

https://huagongshe.com/reaction/514599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 66765094HCID 66765094—
ReactantCarbamic acid, N-[4-(aminooxy)butyl]-, phenylmethyl esterHCID 86695045—
SolventIsopropanolHCID 3776—
ProductHCID 66765490HCID 6676549076.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

N-(4-Chloroquinolin-3-yl)valeramide (1.97 g), benzyl (4-aminooxybutyl)carbamate (2.99 g), triethylamine (0.89 g) and 2-propanol (40.69 g) were combined and heated at 80° C. for 3.5 hours. The reaction was cooled to room temperature, filtered, and the filtrate concentrated under reduced pressure. Dichloromethane (20 mL) was added to the resulting solid and the mixture was stirred for twenty minutes. Undissolved solid was removed by filtration and the filtrate was washed with two 10 mL portions of water that had been made slightly acidic by the addition of 20 drops of hydrochloric acid (1.2 M). The organic fraction was dried and concentrated under reduced pressure. The crude solid was recrystallized from tetrahydrofuran to provide 2.56 g of benzyl 4-{[2-butyl-1H-imidazo[4,5-c]quinolin-1-yl]oxy}butylcarbamate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09107958B2
Source datasetuspto-grants-2015_08
ORD IDord-7578511be90d4fff81ba900a19c9a360
Source noteuspto-grants-2015_08