Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378025Generated: October 31, 2026

o-Bis(bromomethyl)benzene → HCID 53768906, compound

https://huagongshe.com/reaction/1378025

Reaction equation

Participants

RoleNameHCIDCharge
Reactanto-Bis(bromomethyl)benzeneHCID 66665—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 53887943HCID 53887943—
SolventDichloromethaneHCID 6344—
ProductHCID 53768906HCID 5376890662.3%

Reaction Steps

5 g (14 mmol) of (S)-1-(3-aminomethyl-1,2,4-oxadiazol-5-yl)-8-chloro-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepin-9-one, 50 ml of methylene chloride, 12 ml (70 mmol) of N-ethyldiisopropylamine and 3.7 g (14 mmol) of α,α'-dibromo-o-xylene were stirred at room temperature for 72 hours. The reaction solution was washed three times with water, dried over magnesium sulfate and evaporated. The residue was chromatographed on 70 g of silica gel while eluting with methylene chloride/ethyl acetate 7/3. There were obtained 4.0 g (62%) of (S)-8-chloro-12,12a-dihydro-1-(3-isoindolin-2-ylmethyl-1,2,4-oxadiazol-5-yl)-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepin-9-one, which was converted into the hydrochloride of m.p. 170°-175°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665718
Source datasetuspto-grants-1997_09
ORD IDord-cffea1e00ab14c9d8ba2e6f3e3873192
Source noteuspto-grants-1997_09