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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2351441Generated: November 1, 2026

Hydrogen Bromide → 5,11-Dihydro-11-[[[2-[2-[(dipropylamino)methyl]-piperidin-l-yl]ethy]amino]carbonyl]-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one hydrobromide

https://huagongshe.com/reaction/2351441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantAF-DX-384HCID 119357—
SolventEthanolHCID 702—
Product5,11-Dihydro-11-[[[2-[2-[(dipropylamino)methyl]-piperidin-l-yl]ethy]amino]carbonyl]-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one hydrobromideHCID 67935545—

Reaction Steps

A solution of 0.957 g (0.002 mol) of 5,11-dihydro-11-[[[2-[2-[(dipropylamino)methyl]-piperidin-l-yl]ethyl]amino]carbonyl]-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one in 20 ml of ethanol was combined with 0.135 ml of a 45% aqueous hydrobromic acid solution (0.002 mol). The colourless salt mentioned above slowly crystallised out of the mixture and after being left to stand for 3 hours it was suction filtered, washed thoroughly three times with 3 ml of anhydrous ethanol and finally dried at 50° C. in a circulating air dryer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04873236
Source datasetuspto-grants-1989_10
ORD IDord-08ae2f68e9214de2a09c5b94c1bf956b
Source noteuspto-grants-1989_10