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【结 构 式】

【药物名称】Ebselen, DR-3305, PZ-51, Harmokisane

【化学名称】2-Phenyl-1,2-benzisoselenazol-3(2H)-one

【CA登记号】60940-34-3

【 分 子 式 】C13H9NOSe

【 分 子 量 】274.18278

【开发单位】Aventis Pharma (Originator), Daiichi Pharmaceutical (Licensee)

【药理作用】Antiallergy/Antiasthmatic Drugs, Asthma Therapy, CARDIOVASCULAR DRUGS, Cerebrovascular Diseases, Treatment of, NEUROLOGIC DRUGS, RESPIRATORY DRUGS, Restenosis Treatment of, Stroke, Treatment of, Treatment of Disorders of the Coronary Arteries and Atherosclerosis, Antioxidants, NADPH Oxidase Inhibitors, Protein Kinase C (PKC) Inhibitors

合成路线1

A new synthesis of ebselen has been published: The radical reaction of 2-(benzylseleno)-N-phenylbenzamide (I) with triphenyltin hydride (II) and AIBN in refluxing benzene gives N-phenyl-2-(triphenylstannylseleno)benzamide (III), which is treated with dibenzoyl peroxide (IV) in refluxing benzene to yield the diselenide (V). Finally, the diselenide (V) was treated with di-tert-butyl peroxide (VI) in chlorobenzene at 120 C. This reaction cannot be carried out in refluxing benzene due to the extreme insolubility of (V) in benzene.

1 Fong, M.C.; Schiesser, C.H.; Reactions of 2,2'-diselenobis(N-alkylbenzamides) with peroxides: A free-radical synthesis of ebselen and related analogues. Tetrahedron Lett 1995, 36, 40, 7329.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 10245 2-(Benzylselanyl)-N-phenylbenzamide C20H17NOSe 详情 详情
(III) 10246 N-Phenyl-2-[(triphenylstannyl)selanyl]benzamide C31H25NOSeSn 详情 详情
(V) 10247 2-[([[2-(Anilinocarbonyl)phenyl]selanyl]methyl)selanyl]-N-phenylbenzamide C27H22N2O2Se2 详情 详情

合成路线2

A new synthesis of ebselen has been reported: The reaction of benzanilide (I) first with lithium diisopropylamide and then with butyllithium in THF gives the dianion (II), which is treated with freshly sublimed selenium to afford the insertion dianion (III). Finally, this compound is cyclized with CuBr2 in the same solvent. This reaction has also been carried out with 77Se in order to obtain labeled ebselen.

1 Oppenheimer, J.; Silks, L.A.; Synthesis of 2-phenyl-1,2-benziso[Se-77]selenazol-3(2H)-one: 'Ebselen'. J Label Compd Radiopharm 1996, 38, 3, 281.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 10248 N-Phenylbenzamide; Benzanilide 93-98-1 C13H11NO 详情 详情
(II) 10249 2-Lithio-N-phenylbenzenecarboximidic acid lithium salt C13H9Li2NO 详情 详情
(III) 10250 2-Selanyl-N-phenylbenzenecarboximidic acid dilithium salt C13H9Li2NOSe 详情 详情

合成路线3

The neutralized diazonium salt of anthranilic acid (I) is treated with sodium diselenide yielding diselenosalicylic acid (II), which is treated with thionyl chloride to give the selenenyl chloride (III). Treatment of (III) with aniline (IV) in the presence of a base affords PZ-51.

1 Renson, M.; Etschenberg, E.; Winkelmann, J. (A. Nattermann & Cie. GmbH); 2-Phenyl-1,2-benzisoselenazol-3(2H)-one containing pharmaceutical preparations and process for the treatment or rheumatic diseases. DE 3027073; EP 0044971; JP 8256427; US 4352799 .
2 Graf, E.; Dereu, N.; Ebselen. Drugs Fut 1984, 9, 10, 741.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 30590 2-carboxybenzenediazonium chloride C7H5ClN2O2 详情 详情
(II) 30591 2-[2-(2-carboxyphenyl)diselanyl]benzoic acid C14H10O4Se2 详情 详情
(III) 30592 2-(chloroselanyl)benzoyl chloride C7H4Cl2OSe 详情 详情
(IV) 12294 Aniline; Phenylamine 62-53-3 C6H7N 详情 详情
Extended Information