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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 598294Generated: October 27, 2026

Methanol → 1-(7-Benzyloxy-3-nitroquinolin-4-ylamino)-2-methylpropan-2-ol

https://huagongshe.com/reaction/598294

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTriethylamineHCID 8471—
ReactantN-(2-methylpropyl)hydroxylamineHCID 9543329—
Reactant7-(Benzyloxy)-4-chloro-3-nitroquinolineHCID 21075751—
Product1-(7-Benzyloxy-3-nitroquinolin-4-ylamino)-2-methylpropan-2-olHCID 67051017—

Reaction Steps

Triethylamine (81.3 g, 0.803 mol) was added to a solution of 230.0 g (0.731 mol) of 7-benzyloxy-4-chloro-3-nitroquinoline (230.0 g, 0.731 mmol), prepared in Parts A-D of Example 1, in methanol (1.84 L). Hydroxyisobutylamine (71.6 g, 0.803 mol) was then added over a period of five minutes; the temperature rose from 30° C. to 39° C. during the addition. The reaction mixture was heated at reflux for four hours and then allowed to cool to room temperature. The solid product was isolated by filtration, washed with ethanol (1 L), and dried under vacuum at 55° C. to provide 261.2 g of 1-[(7-benzyloxy-3-nitroquinolin-4-yl)amino]-2-methylpropan-2-ol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07897597B2
Source datasetuspto-grants-2011_03
ORD IDord-4fe4e0a93777480c9fd2c26b7b619fea
Source noteuspto-grants-2011_03