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【结 构 式】

【药物名称】BIA-3-202

【化学名称】1-(3,4-Dihydroxy-5-nitrophenyl)-2-phenyl-1-ethanone

【CA登记号】274925-86-9

【 分 子 式 】C14H11NO5

【 分 子 量 】273.24747

【开发单位】Bial (Originator), Portela (Originator)

【药理作用】Antiparkinsonian Drugs, Extrapyramidal Disorders, Treatment of, NEUROLOGIC DRUGS, COMT Inhibitors

合成路线1

Protection of vanillin (I) as the benzyl ether (II), followed by reaction with benzylmagnesium bromide, furnished alcohol (III). Oxidation of alcohol (III) to the corresponding ketone (IV) was achieved by means of chromium trioxide or, in an improved procedure, by Oppenauer oxidation with cyclohexanone and sodium tert-butoxide. Benzyl group cleavage in (IV) either with HBr, or by transfer hydrogenolysis, yielded phenol (V). Regioselective nitration of (V) gave the ortho-nitrophenol (VI). The title compound was finally obtained by methyl ether cleavage in (VI) with boiling HBr or with AlCl3 in pyridine.

1 Benes, J.; Vieira-Coelho, M.A.; Borges, N.; Freitas, A.P.; Soares-da-Silva, P.; Alves, P.C.; Learmonth, D.A.; Synthesis of 1-(3,4-dihydroxy-5-nitrophenyl)-2-phenyl-ethanone and derivatives as potent and long-acting peripheral inhibitors of catechol-O-methyltransferase. J Med Chem 2002, 45, 3, 685.
3 Benes, J.; Soares da Silva, P.M.V.A.; Learmonth, D.A. (Portela & Ca., SA); Substd. 2-phenyl-1-(3,4-dihydroxy-5-nitrophenyl)-1-ethanones, their use in the treatment of some central and peripheral nervous system disorders and pharmaceutical compsns. containing them. EP 1010688; GB 2344819; WO 0037423 .
2 Learmonth, D.; et al.; Synthesis of 1-(3,4-dihydroxy-5-nitrophenyl)-2-phenyl-ethanone and derivatives as potent and selective inhibitors of catechol-O-methyltransferase (COMT). 16th Int Symp Med Chem (Sept 18 2000, Bologna) 2000, Abst PA-34.
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) 22701 4-hydroxy-3-methoxybenzaldehyde 121-33-5 C8H8O3 详情 详情
(II) 14045 4-(Benzyloxy)-3-methoxybenzaldehyde; 4-Benzyloxy-3-methoxybenzaldehyde 2426-87-1 C15H14O3 详情 详情
(III) 59403 1-[4-(benzyloxy)-3-methoxyphenyl]-2-phenyl-1-ethanol C22H22O3 详情 详情
(IV) 59404 1-[4-(benzyloxy)-3-methoxyphenyl]-2-phenyl-1-ethanone C22H20O3 详情 详情
(V) 59405 1-(4-hydroxy-3-methoxyphenyl)-2-phenyl-1-ethanone C15H14O3 详情 详情
(VI) 59406 1-(4-hydroxy-3-methoxy-5-nitrophenyl)-2-phenyl-1-ethanone C15H13NO5 详情 详情
Extended Information