HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737378Generated: November 1, 2026
1,3-Dichloroacetone → 7-chloro-3-(4-chloromethyl-thiazol-2-yl)-8-fluoro-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one
https://huagongshe.com/reaction/1737378
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Dichloroacetone | HCID 10793 | — |
| Reactant | HCID 21842257 | HCID 21842257 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 7-chloro-3-(4-chloromethyl-thiazol-2-yl)-8-fluoro-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one | HCID 21842292 | 35.1% |
Reaction Steps
A yellow suspension of 2.45 g (0.00754 mol) of 7-chloro-8-fluoro-5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepine-3-thiocarboxamide in 130 ml of dioxan was treated with 1.05 g (0.00829 mol) of 1,3-dichloro-2-propanone. The suspension was boiled at reflux for 20 hrs. and cooled. A further 1.05 g (0.00829 mol) of 1,3-dichloro-2-propanone and 60 ml of dioxan were added and the solution was boiled at reflux for a further 16 hrs. The solution was cooled and completely freed from the solvents. The residue was chromatographed over silica gel with cyclohexane/ethyl acetate 1:2 as the eluent and recrystallized from hot acetonitrile. There were obtained 1.05 g (35%) of 7-chloro-3-(4-chloromethyl-thiazol-2-yl)-8-fluoro-5-methyl-5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-one as white crystals; m.p. 234-235°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05962450 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-9b70422eff9948a3a6fdae9369098fd2 |
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| Source note | uspto-grants-1999_10 |
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