Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540296Generated: October 29, 2026

2,4-Dichloro-6-methylquinoline → (E)-2-(4-chloro-6-methylquinolin-2-yl)-N-methoxy-3,4-dihydro-1H-2-benzazepin-5-imine

https://huagongshe.com/reaction/540296

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-6-methylquinolineHCID 2754668—
Reactant2-(4-chloro-6-methylquinolin-2-yl)-5,5-difluoro-2,3,4,5-tetrahydro-1H-benzazepineHCID 71255094—
ReactantN-methoxy-1,2,3,4-tetrahydro-5H-2-benzazepin-5-imineHCID 86691438—
ReactantN-[(3-aminooxetan-3-yl)methyl]-2-[(5E)-5-methoxyimino-3,4-dihydro-1H-2-benzazepin-2-yl]-6-methylquinolin-4-amineHCID 89406081—
Product(E)-2-(4-chloro-6-methylquinolin-2-yl)-N-methoxy-3,4-dihydro-1H-2-benzazepin-5-imineHCID 89406036—

Reaction Steps

The title compound was prepared in analogy to 2-(4-chloro-6-methylquinolin-2-yl)-5,5-difluoro-2,3,4,5-tetrahydro-1H-benzazepine in Example 110-1 in Scheme 56 by using 2,4-dichoro-6-methylquinoline and N-methoxy-1,2,3,4-tetrahydro-5H-2-benzazepin-5-imine. N-[(3-Aminooxetan-3-yl)methyl]-2-[(5E)-5-(methoxyimino)-1,3,4,5-tetrahydro-2H-2-benzazepin-2-yl]-6-methylquinolin-4-amine

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871756B2
Source datasetuspto-grants-2014_10
ORD IDord-11fbfbfcdc024069ace7c9145850fe27
Source noteuspto-grants-2014_10