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【结 构 式】

【分子编号】55222

【品名】3,6-Dichlorophthalic anhydride

【CA登记号】

【 分 子 式 】C8H2Cl2O3

【 分 子 量 】217.00748

【元素组成】C 44.28% H 0.93% Cl 32.67% O 22.12%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(VIII)

This compound has been obtained by two different methods: The reduction of 1,4-diamino-5,8-dihydroxyanthraquinone (I) or 1,5-diamino-4,8-dihydroxyanthraquinone (II) with Na2S2O4 and NaOH in water gives the leuco derivative (III), which is condensed with N,N-dimethylethylene-1,2-diamine (IV) in refluxing ethanol and reoxidized by air to yield 1,4-bis[2-(dimethylamino)ethylamino]-5,8-dihydroxyanthraquinone (V). Finally, this compound is treated with MCPBA in dichloromethane to afford the target bis-N-oxide. Alternatively, the reduction of tetrachlorophthalic anhydride (VI) with Zn and NaOH in water at 50-60 C gives 3,4,6-trichlorophthalic anhydride (VII), which is further reduced with Zn and NaOH in refluxing water to yield 3,6-dichlorophthalic anhydride (VIII). The reaction of (VIII) with KF and NaF at 260-27 ?C affords 3,6-difluorophthalic anhydride (IX), which is cyclized with hydroquinone (X) by means of AlCl3 and NaCl at 200 +/- 5 C to provide 1,4-difluoro-5,8-dihydroxyanthraquinone (XI). Finally, this compound is condensed with N,N-dimethylethylene-1,2-diamine (IV) in pyridine to afford the already reported 1,4-bis[2-(dimethylamino)ethylamino]-5,8-dihydroxyanthraquinone (V), which is oxidized with MCPBA as before.

1 Chang, P.; Chang, C.C.; An improved practical synthesis of leuco-1,4,5,8-tetrahydroxyanthraquinone. Synth. Commun. 1995, 25, 3, 1893.
2 Denny, W.A.; Lee, H.H.; A large-scale synthesis of the bioreductive drug 1,4-bis[[2-(dimethylamino)ethyl]amino]-5,8-dihydroxyanthracene-9,10-dione bis-N-oxide (AQ4N). J Chem Soc - Perkins Trans I 1999, 19, 2755.
3 Patterson, L.H. (National Research Development Corp.); Anti-cancer cpds.. US 5132327; WO 9105824 .
4 Denny, W.A.; Lee, H.H. (BTG International Ltd.); Process for the preparation of 1,4-bis[[2-(dimethylamino)ethyl]amino]-5,8-dihydroxyanthracene-9,10-dione. WO 0005194 .
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) 55217 1,4-diamino-5,8-dihydroxyanthra-9,10-quinone C14H10N2O4 详情 详情
(II) 55218 1,5-diamino-4,8-dihydroxyanthra-9,10-quinone C14H10N2O4 详情 详情
(III) 55219 1,4,5,8-tetrahydroxy-2,3-dihydro-9,10-anthracenedione C14H10O6 详情 详情
(IV) 14881 N-(2-aminoethyl)-N,N-dimethylamine; N(1),N(1)-dimethyl-1,2-ethanediamine; 2-Dimethylaminoethylamine 108-00-9 C4H12N2 详情 详情
(V) 55220 1,4-bis{[2-(dimethylamino)ethyl]amino}-5,8-dihydroxyanthra-9,10-quinone C22H28N4O4 详情 详情
(VI) 51351 Tetrachlorophthalic anhydride; 4,5,6,7-Tetrachloro-1,3-isobenzofurandione 117-08-8 C8Cl4O3 详情 详情
(VII) 55221 4,5,7-trichloro-2-benzofuran-1,3-dione C8HCl3O3 详情 详情
(VIII) 55222 3,6-Dichlorophthalic anhydride C8H2Cl2O3 详情 详情
(IX) 55223 3,6-Difluorophthalic anhydride C8H2F2O3 详情 详情
(X) 13163 p-Dihydrobenzene; Hydroquinone 123-31-9 C6H6O2 详情 详情
(XI) 55224 1,4-difluoro-5,8-dihydroxyanthra-9,10-quinone C14H6F2O4 详情 详情
Extended Information