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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244860Generated: October 31, 2026

Triethylamine → 1-[(6-Bromo-3-nitroquinolin-4-yl)amino]-2-methylpropan-2-ol

https://huagongshe.com/reaction/244860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant2-Propanol, 1-amino-2-methyl-HCID 95102—
ReactantHCID 178526759HCID 178526759—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product1-[(6-Bromo-3-nitroquinolin-4-yl)amino]-2-methylpropan-2-olHCID 6907956790.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

Phosphorous oxychloride (5.45 mL, 58.5 mmol) was added to a slurry of 6-bromo-3-nitroquinolin-4-ol (15 g, 55.7 mmol) in N,N-dimethylformamide (100 mL). The reaction mixture was heated to 100° C. for 10 minutes and then cooled to ambient temperature. The solution was poured into ice water (400 mL) and stirred for 20 minutes. The resulting precipitate was filtered, washed with water, and dried. The recovered solid was transferred to a round bottomed flask and tetrahydrofuran (100 mL) was added. A solution of triethylamine (11.6 mL, 83.5 mmol) and 1-amino-2-methylpropan-2-ol (5.21 g, 58.5 mmol) in tetrahydrofuran (20 mL) was added dropwise. The reaction was stirred for 16 hours. The mixture was poured into water and stirred for 15 minutes. The resulting yellow solid was filtered and dried to provide 17.2 g of 1-[(6-bromo-3-nitroquinolin-4-yl)amino]-2-methylpropan-2-ol as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658666B2
Source datasetuspto-grants-2014_02
ORD IDord-7bb46d0d6a264e188e728b1f86290709
Source noteuspto-grants-2014_02