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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110937Generated: November 2, 2026

7-Chloro-5,6-dihydro-6-oxo-4H-imidazo[1,5-a]-[4,1]benzoxazepine-3-amidoxime → 7-Chloro-3-(5-propyl-1,2,4-oxadiazol-3-yl)-5,6-dihydro-6-oxo-4H-imidazo[1,5-a][4,1]benzoxazepine

https://huagongshe.com/reaction/1110937

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-Chloro-5,6-dihydro-6-oxo-4H-imidazo[1,5-a]-[4,1]benzoxazepine-3-amidoximeHCID 53746886—
SolventButyric anhydrideHCID 7798—
Product7-Chloro-3-(5-propyl-1,2,4-oxadiazol-3-yl)-5,6-dihydro-6-oxo-4H-imidazo[1,5-a][4,1]benzoxazepineHCID 5407969599.5%

Reaction Steps

7-Chloro-5,6-dihydro-6-oxo-4H-imidazo[1,5-a]-[4,1]benzoxazepine-3-amidoxime (2 g, 7 mmole) in n-butyric anhydride (6 ml) was heated at 150° C. for 1 hour. The crude product was chromatographed on silica, initially with ethyl acetate:hexane (1:1) and then changing to ethyl acetate. The purified product was crystallised from ethyl acetate:cyclohexane (4:1) to give the product (1.2 g, 50%), m.p. 130°-132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04977258
Source datasetuspto-grants-1990_12
ORD IDord-aa1ca97b95f6411d9789bf38761b10d1
Source noteuspto-grants-1990_12