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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1692607Generated: October 29, 2026

HCID 23002992, compound → 7-Chloro-8-morpholin-4-yl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepine monohydrobromide

https://huagongshe.com/reaction/1692607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23002992HCID 23002992—
Reactanttert-butyl 7-chloro-8-morpholin-4-yl-2,3-dihydropyrido[3,2-f][1,4]oxazepine-4(5H)-carboxylateHCID 67279788—
SolventEthanolHCID 702—
Product7-Chloro-8-morpholin-4-yl-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepine monohydrobromideHCID 6728022825%

Reaction Steps

To a solution of the compound (0.10 g) obtained in step 1 in ethanol (1 mL) was added hydrobromic acid-ethanol solution (1 mL), and the mixture was stirred at room temperature for 4 hr. The solvent was evaporated under reduced pressure, and the aqueous layer was made basic with ethyl acetate and aqueous sodium hydroxide solution. The organic layer was washed with brine and dried, and the solvent was evaporated under reduced pressure. Ethyl acetate was added to the residue, and hydrobromic acid-ethanol solution was added. The precipitate was collected by filtration to give the title compound (0.03 g, 25%) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158617B2
Source datasetuspto-grants-2012_04
ORD IDord-46e55518a98a4a57b21a3df181202d8b
Source noteuspto-grants-2012_04