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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540802Generated: October 26, 2026

Ammonium Hydroxide → Oxane-4-carboxamide

https://huagongshe.com/reaction/540802

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant2H-Pyran-4-carboxylic acid, tetrahydro-, methyl esterHCID 2773520—
ReactantBenzyloxy-4-chloro-3-nitroquinolineHCID 21075762—
ReactantBenzyloxy-3-nitroquinolin-4-amineHCID 66649911—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductOxane-4-carboxamideHCID 13197203—

Reaction Steps

In step (5) of Reaction Scheme I, a benzyloxy-4-chloro-3-nitroquinoline of Formula XIX is treated with an amine of Formula R1—NH2 to provide a benzyloxy-3-nitroquinolin-4-amine of Formula XX. The reaction is conveniently carried out by adding the amine of Formula R1—NH2 to a solution of the benzyloxy-4-chloro-3-nitroquinoline of Formula XIX in a suitable solvent such as dichloromethane or methanol in the presence of a tertiary amine such as triethylamine. The reaction can be carried out at ambient temperature or at an elevated temperature such as, for example, the reflux temperature of the solvent. The reaction product can be isolated using conventional methods. Several mines of Formula R1—NH2 are commercially available; others can be prepared by known synthetic methods. For example, methyl tetrahydro-2H-pyran-4-carboxylate treated with ammonium hydroxide to form tetrahydro-2H-pyran-4-carboxamide, which can then be reduced with lithium aluminum hydride to provide tetrahydro-2H-pyran-4-ylmethylamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871782B2
Source datasetuspto-grants-2014_10
ORD IDord-ce9fce475629448ab676fa3dcd87db44
Source noteuspto-grants-2014_10