HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378004Generated: November 1, 2026
o-Bis(bromomethyl)benzene → HCID 53888344, compound
https://huagongshe.com/reaction/1378004
Participants
| Role | Name | HCID | Charge |
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| Reactant | o-Bis(bromomethyl)benzene | HCID 66665 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 54208158 | HCID 54208158 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 53888344 | HCID 53888344 | 33.8% |
Reaction Steps
3.56 g (10 mmol) of (S)-1-(5-aminomethyl-1,2,4-oxadiazol-3-yl)-8-chloro-12,12a-dihydro-9H,11H-azeto[2,1-c]imidazo[1,5-a][1,4]benzodiazepin-9-one, 15 ml of methylene chloride, 8.6 ml (50 mmol) of N-ethyldiisopropylamine and 2.64 g (10 mmol) of α,α'-dibromo-o-xylene were stirred at room temperature for 20 hours. The reaction solution was washed three times with water, dried over magnesium sulfate and evaporated. The residue was chromatographed on 500 g of silica gel while eluting with methylene chloride/methanol 19/1. There were obtained 1.55 g (33%) of (S)-8-chloro-12,12a-dihydro-1-(5-isoindolin-2-ylmethyl-1,2,4-oxadiazol-3-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. 218°-222°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05665718 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-76819ccfc404440a8a0955d6ab2f3617 |
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| Source note | uspto-grants-1997_09 |
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