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【结 构 式】

【药物名称】Entacapone, COM-998, OR-611, Comtess, Comtan

【化学名称】(E)-2-Cyano-N,N-diethyl-3-(3,4-dihydroxy-5-nitrophenyl)propenamide
      (E)-2-Cyano-N,N-diethyl-3-(3,4-dihydroxy-5-nitrophenyl)acrylamide
      (E)-alpha-Cyano-N,N-diethyl-3,4-dihydroxy-5-nitrocinnamamide

【CA登记号】130929-57-6, 133180-79-7 ([14C]-labeled), 116314-67-1 (undefined stereoch.)

【 分 子 式 】C14H15N3O5

【 分 子 量 】305.29275

【开发单位】Orion Corp. (Originator), Novartis (Licensee), Bristol-Myers Squibb (Comarketer)

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

合成路线1

 

1 Backstrom RJ, Heinola KE, et aL 1990. Pharmacologunlly active compmmds. metbods for the preparation thereof and compositions containing the same. US 4963590
2 Pippuri AK, Honkanen EJ, et aL 1992. Stable polymorphic form of (E)-N,N-diethyl-2-cyano-3-(3,4-dihydroxy-5-nitrophenyl) acrylamide and the process for its prepantion. US 5135950
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) 66317 5-Nitrovanillin;4-Hydroxy-3-methoxy-5-nitrobenzaldehyde 6635-20-7 C8H7NO5 详情 详情
(II) 15282 3,4-dihydroxy-5-nitrobenzaldehyde 116313-85-0 C7H5NO5 详情 详情
(III) 15283 2-cyano-N,N-diethylacetamide 26391-06-0 C7H12N2O 详情 详情

合成路线2

 

1 Jasti V.Veera Reddy A, et aL 2005. Catalytic aldol condensation and acid hydrolysis process for the preparation of cntacapone from 3-alkoxy4-hydroxy-5-nitrobenzadehyde ruul N, N-diethyl-2-cyanoacetamide. W0 2005063693
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) 66317 5-Nitrovanillin;4-Hydroxy-3-methoxy-5-nitrobenzaldehyde 6635-20-7 C8H7NO5 详情 详情
(II) 15283 2-cyano-N,N-diethylacetamide 26391-06-0 C7H12N2O 详情 详情
(III) 66318 2-cyano-N,N-diethyl-3-(4-hydroxy-3-methoxy-5-nitrophenyl)acrylamide   C15H17N3O5 详情 详情

合成路线3

 

1 Cziaky Z 2006.Process for the preparation of entacapone in a stable polymorphic form and preparation of intermediates for its preparation. W0 2006064296
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) 15283 2-cyano-N,N-diethylacetamide 26391-06-0 C7H12N2O 详情 详情
(III) 66319 2-cyano-N,N-diethyl-3-(4-hydroxy-3-methoxyphenyl)acrylamide   C15H18N2O3 详情 详情
(IV) 66318 2-cyano-N,N-diethyl-3-(4-hydroxy-3-methoxy-5-nitrophenyl)acrylamide   C15H17N3O5 详情 详情

合成路线4

Title compound is obtained by reaction of 3,4-dihydroxy-5-nitrobenzaldehyde (I) with N,N-diethyl-2-cyanoacetamide (II) in the presence of piperidine acetate in ethanol.

1 Backstrom, R.J.; Heinola, K.E.; Honkanen, E.J.; Kaakkola, S.K.; Karrisalo, P.J.; Linden, I.-B.Y.; Mannisto, P.T.; Nissinen, E.A.O.; Pohto, P.; Pippuri, A.K.; Pystynen, J.J. (Orion Corporation); Novel pharmacologically active cpds., their process of preparation and compsns. containing them. AU 8781879; BE 1003279; CH 685436; DE 3740383; FR 2607493; GB 2200109; JP 1988170311; US 4963590; US 5112861 .
2 Castaner, J.; Prous, J.; Rabasseda, X.; Entacapone. Drugs Fut 1994, 19, 7, 641.
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) 15282 3,4-dihydroxy-5-nitrobenzaldehyde 116313-85-0 C7H5NO5 详情 详情
(II) 15283 2-cyano-N,N-diethylacetamide 26391-06-0 C7H12N2O 详情 详情
Extended Information