HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 328498Erstellt: 25. Oktober 2026
Clonazepam → 11b-(2-chlorophenyl)-10-nitro-2,3,5,11b-tetrahydrooxazolo[3,2-d][1,4]benzodiazepin-6(7H)-one
https://huagongshe.com/reaction/328498
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Clonazepam | HCID 2802 | — |
| Edukt | Ethylene Oxide | HCID 6354 | — |
| Edukt | Ammonium Hydroxide | HCID 14923 | — |
| Lösungsmittel | 1,2-Dichloroethane | HCID 11 | — |
| Produkt | 11b-(2-chlorophenyl)-10-nitro-2,3,5,11b-tetrahydrooxazolo[3,2-d][1,4]benzodiazepin-6(7H)-one | HCID 12317902 | — |
Reaktionsschritte
A solution of 5.2 g (0.02 M) of stannic chloride in 60 ml of dry ethylene dichloride under nitrogen was treated with 2.9 g (0.0091 M) of 5-(2-chlorophenyl)-1,3-dihydro-7-nitro-2H-1,4-benzodiazepin-2-one. The reaction was cooled in an ice bath, and 2.6 g (0.06 M) of ethylene oxide in 10 ml of ethylene dichloride was added with stirring over an 8 min period. After 18 hr at room temperature, the solution was made basic with concentrated ammonium hydroxide and filtered. The filtrates were washed with a saturated solution of brine, dried over anhydrous sodium sulfate and evaporated to dryness. The residue was crystallized from a mixture of dichloromethane, methanol and petroleum ether to give the above named product as white rods, melting at 201°-203° .
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04017532 |
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| Quelldatensatz | uspto-grants-1977_04 |
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| ORD ID | ord-ebeb7e760c434744a6d05b75d2b8ca5d |
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| Quellennotiz | uspto-grants-1977_04 |
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