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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818207Generated: October 27, 2026

Triethylamine → 1-(6-Benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol

https://huagongshe.com/reaction/1818207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Propanol, 1-amino-2-methyl-HCID 95102—
Reactant7-Benzyl-4-chloro-3-nitroquinolineHCID 21984193—
Reactant6-Benzyl-4-chloro-3-nitroquinolineHCID 21984226—
SolventDichloromethaneHCID 6344—
Product1-(6-Benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-olHCID 21984410—
Product1-(7-Benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-olHCID 21984452—

Reaction Steps

Under a nitrogen atmosphere, 1-amino-2-methylpropan-2-ol (1.2 equivalents) was added to a 0.2 M solution of 7-benzyl-4-chloro-3-nitroquinoline or 6-benzyl-4-chloro-3-nitroquinoline (1 equivalent) and triethylamine (3 equivalents) in dichloromethane, and the reaction was stirred overnight at ambient temperature. The volatiles were removed under reduced pressure, and the residue was stirred with water (50 mL) for one hour. The resulting yellow solid was isolated by filtration and washed with water to provide 1-(7-benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol or 1-(6-benzyl-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol, respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598382B2
Source datasetuspto-grants-2009_10
ORD IDord-bede23847f854d9aa689be3226ba2428
Source noteuspto-grants-2009_10