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【结 构 式】

【分子编号】49254

【品名】4,5-dichloro-2-iodoaniline; tert-butyl(dimethyl)[3-(tetrahydro-2H-pyran-2-yloxy)-1-propynyl]silane

【CA登记号】

【 分 子 式 】C14H26O2Si

【 分 子 量 】254.44474

【元素组成】C 66.09% H 10.3% O 12.58% Si 11.04%

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:(II)

The reaction of the propargyl tetrahydropyranyl ether (I) with TBDMS-Cl and BuLi in THF gives the silylated acetylene (II), which is treated with Br2 and PPh3 to yield the silylated propargyl bromide (III). The reaction of (III) with the pyranopyridone (IV) by means of NaH and LiBr in DMF/DME affords the alkylated pyranopyridone (V), which is cyclized with 4-acetoxyphenyl isocyanide (VI) by means of hexamethyldistannane in refluxing benzene to provide the silylated acetoxycamptothecin (VII). Finally, this compound is deacetylated with K2CO3 in methanol.

1 Bom, D.; et al.; The novel silatecan 7-tert-butyldimethylsilyl-10-hydroxycamptothecin displays high lipophilicity, improved human blood stability, and potent anticancer activity. J Med Chem 2000, 43, 21, 3970.
2 Bom, D.; Curran, D.P.; Josien, H. (University of Pittsburgh); Camptothecin analogs and methods of preparation thereof. EP 1017399; JP 2001513567; US 6150343; WO 9909996 .
3 Bom, D.; Curran, D.P.; Josien, H.; Burke, T.G. (University of Pittsburgh); Camptothecin analogs and methods of preparation thereof. WO 0035924 .
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) 43853 (1S,5S,7R,10S,12S,16S)-3,3-di(tert-butyl)-16-[[tert-butyl(dimethyl)silyl]oxy]-15,18,18-trimethyl-2,4-dioxa-3-silatetracyclo[12.3.1.0(1,5).0(6,11)]octadeca-6(11),14-diene-7,10,12-triol C32H58O6Si2 详情 详情
(II) 49254 4,5-dichloro-2-iodoaniline; tert-butyl(dimethyl)[3-(tetrahydro-2H-pyran-2-yloxy)-1-propynyl]silane C14H26O2Si 详情 详情
(III) 35102 (3-bromo-1-propynyl)(tert-butyl)dimethylsilane C9H17BrSi 详情 详情
(IV) 49255 (4S)-4-ethyl-4-hydroxy-6-iodo-1H-pyrano[3,4-c]pyridine-3,8(4H,7H)-dione C10H10INO4 详情 详情
(V) 49256 (4S)-7-[3-[tert-butyl(dimethyl)silyl]-2-propynyl]-4-ethyl-4-hydroxy-6-iodo-1H-pyrano[3,4-c]pyridine-3,8(4H,7H)-dione C19H26INO4Si 详情 详情
(VI) 49257   C9H7NO2 详情 详情
(VII) 49258 (4S)-11-[tert-butyl(dimethyl)silyl]-4-ethyl-4-hydroxy-3,14-dioxo-3,4,12,14-tetrahydro-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-9-yl acetate C28H32N2O6Si 详情 详情
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