HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704553Generated: October 30, 2026
Clobazam → 7-chloro-1-methyl-5-phenyl-1H-1,5-benzodiazepin-2,3,4(5H)-trione 3-oxime
https://huagongshe.com/reaction/704553
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Clobazam | HCID 2789 | — |
| Reactant | tert-Pentyl nitrite | HCID 243476 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 7-chloro-1-methyl-5-phenyl-1H-1,5-benzodiazepin-2,3,4(5H)-trione 3-oxime | HCID 53769573 | 85% |
Reaction Steps
3 g of 7-chloro-1-methyl-5-phenyl-1H-1,5-benzodiazepine-2,4(3H,5H)-dione were suspended in 30 ml of tert-butanol and 1.12 g of potassium tert-butylate were added in small fractions. While maintaining the temperature at 20° C. with a water bath, 2.3 ml of tert-amyl nitrite were added and the solution thickened and a precipitate formed. After standing for 16 hours at ambient temperature, the precipitate formed was separated off (potassium salt of the oxime) and dissolved in 20 ml of water and acidified by acetic acid. The precipitate formed was extracted and the organic phase was washed with water, dried and concentrated to obtain 2.8 g of the expected product (yield=85%) melting at approx. 50° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04988692 |
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| Source dataset | uspto-grants-1991_01 |
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| ORD ID | ord-8a76da38036143bd8d919af7f566e943 |
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| Source note | uspto-grants-1991_01 |
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