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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1803384Generated: November 1, 2026

Triethylamine → HCID 58527483, compound

https://huagongshe.com/reaction/1803384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantIsobutyryl chlorideHCID 62325—
ReactantHCID 67435646HCID 67435646—
SolventDichloromethaneHCID 6344—
ProductHCID 58527483HCID 5852748334%

Reaction Conditions

Temperature0 °C

Reaction Steps

(11S)-11-(3-Aminopropyl)-10,11-dihydro-8H-[1,4]oxazino[4′,3′:1,2]imidazo[4,5-c]quinolin-6-amine (190 mg, 0.640 mmol) was dissolved in 8 mL of CH2Cl2 and the reaction mixture was cooled to 0° C. under N2. Triethylamine (356 μL, 2.56 mmol) was added followed by iso-butyryl chloride (67 μL, 0.643 mmol). After stirring overnight, the reaction mixture was diluted with 20 mL of CH2Cl2 and was washed successively with saturated NaHCO3 solution, H2O and brine. The organic portion was dried over Na2SO4, filtered and concentrated under reduced pressure. Chromatography (SiO2, 10% methanol/CHCl3) gave a white solid. Crystallization from ethyl acetate gave N-{3-[(11S)-6-amino-10,11-dihydro-8H-[1,4]oxazino[4′,3′:1,2]imidazo[4,5-c]quinolin-11-yl]propyl}-2-methylpropanamide (80 mg) as a white solid, mp 207-208° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08350034B2
Source datasetuspto-grants-2013_01
ORD IDord-a3c9ca66b58e418ca426623be9cffed9
Source noteuspto-grants-2013_01