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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 17854Generated: October 27, 2026

Bromine → 3,7-dibromo-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one

https://huagongshe.com/reaction/17854

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant2,3,4,5-tetrahydro-1H-1-benzazepineHCID 576503—
Reactant3-Bromo-1,3,4,5-tetrahydro-2H-1-benzazepin-2-oneHCID 2757184—
SolventAcetic AcidHCID 176—
Product3,7-dibromo-2,3,4,5-tetrahydro-1H-1-benzazepin-2-oneHCID 58857219—

Reaction Steps

Scheme 5 describes an example of bromination of a tetrahydrobenzazepine intermediate. Bromine can be added slowly to commercially available 3-bromo-1,3,4,5-tetrahydro-1-benzazepin-2-one in acetic acid with stirring at room temperature to provide the useful intermediate 3,7-dibromo-1,3,4,5-tetrahydro-1-benzazepin-2-one, which can be used in many transformations described herein. Bromination using similar conditions can be carried out on other amino aryl cores described herein to provide intermediates for transformation to the compounds of the invention described in Schemes 8, 9 and 10.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07741317B2
Source datasetuspto-grants-2010_06
ORD IDord-5dc8d1a4d7a64005aaa34528a13933b9
Source noteuspto-grants-2010_06