HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430661Generated: October 25, 2026
Water → 8-Methoxy-3-methyl-6-phenyl-11H-imidazo[1,2-c][2,3]benzodiazepine
https://huagongshe.com/reaction/430661
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | (2-Methyl-1,3-dioxolan-2-yl)methanamine | HCID 12434663 | — |
| Reactant | 8-methoxy-1-phenyl-4,5-dihydro-3H-2,3-benzodiazepine-4-thione | HCID 17887821 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | 8-Methoxy-3-methyl-6-phenyl-11H-imidazo[1,2-c][2,3]benzodiazepine | HCID 18183158 | — |
Reaction Steps
500 mg of 8-methoxy-1-(phenyl)-4,5-dihydro-3H-2,3-benzodiazepine-4-thione is stirred in 1.5 ml of ethylene glycol monomethyl ether (Cellosolve®) and 548 mg of 2-aminomethyl-2-methyl-1,3-dioxolane while argon is passing through it for 10 hours at 60° C. After filtration and washing with cold ethanol and diisopropyl ether, 550 mg of imino compound, which is dissolved in 10 ml of ethanol, mixed with 10 ml of concentrated hydrochloric acid and refluxed for 3 hours, is obtained. It is added to water, set at pH 11 and extracted with ethyl acetate. The ethyl acetate phase is washed with water, dried, filtered and concentrated by evaporation. After recrystallization from ethyl acetate/diisopropyl ether, 240 mg of 8-methoxy-3-methyl-6-phenyl-11H-imidazo[1,2-c][2,3]benzodiazepine with a melting point of 140° C. is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06323197B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-50f2e2a4e9f640f3a950021f1c6e68e2 |
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| Source note | uspto-grants-2001_11 |
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