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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantClobazamHCID 2789—
Reactanttert-Pentyl nitriteHCID 243476—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
Product7-chloro-1-methyl-5-phenyl-1H-1,5-benzodiazepin-2,3,4(5H)-trione 3-oximeHCID 5376957385%

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04988692
Source datasetuspto-grants-1991_01
ORD IDord-8a76da38036143bd8d919af7f566e943
Source noteuspto-grants-1991_01