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【结 构 式】

【药物名称】Cilomilast, SB-207499, Ariflo

【化学名称】cis-4-Cyano-4-[3-(cyclopentyloxy)-4-methoxyphenyl]cyclohexane-1-carboxylic acid

【CA登记号】153259-65-5

【 分 子 式 】C20H25NO4

【 分 子 量 】343.42655

【开发单位】GlaxoSmithKline (Originator)

【药理作用】Asthma Therapy, Atopic Dermatitis, Agents for, Bronchodilators, Chronic Obstructive Pulmonary Diseases (COPD), Treatment of, DERMATOLOGIC DRUGS, RESPIRATORY DRUGS, Phosphodiesterase IV Inhibitors

合成路线1

The reaction of 3-cyclopentyloxy-4-methoxybenzaldehyde (I) with LiBr, trimethylsilyl chloride (TMS-Cl) and 1,1,3,3-tetramethyldisiloxane in acetonitrile gives the corresponding benzyl bromide (II), which by reaction with NaCN in DMF affords 2-(3-cyclopentyloxy-4-methoxyphenyl)acetonitrile (III). The condensation of (III) with methyl acrylate (IV) by means of Triton B in refluxing acetonitrile yields the 4-cyanopimelate (V), which is cyclized by means of NaH in refluxing DME, giving the 2-oxocyclohexanecarboxylic ester (VI). The decarboxylation of (VI) by means of NaCl in DMSO/water at 150 C yields the cyclohexanone (VII), which is condensed with 2-(trimethylsilyl)-1,3-dithiane (VIII) by means of BuLi in THF, affording the cyclohexylidene-dithiane (IX). The methanolysis of (IX) catalyzed by HgCl2 and HClO4 in refluxing methanol gives a mixture of the cis- and trans-4-cyano-4-(3-cyclopentyloxy-4-methoxyphenyl)cyclohexanecarboxylic acid methyl ester which is submitted to flash chromatography to obtain the cis-isomer (XII). Finally, this compound is hydrolyzed with KOH in methanol/THF/water.

1 Graul, A.; Castañer, J.; Silvestre, J.S.; SB-207499. Drugs Fut 1998, 23, 6, 607.
2 Christensen, S.B.; Forster, C.J.; Guider, A.; et al.; 1,4-Cyclohexanecarboxylates: Potent and selective inhibitors of phosphodiesterase 4 for the treatment of asthma. J Med Chem 1998, 41, 6, 821-35.
3 Bordas-Nagy, J.; Gorycki, P.; Webb, K.S. (SmithKline Beecham plc); Cyano cpds. and preparation thereof. JP 1997510213; WO 9524381 .
4 Christensen, S.B. IV (SmithKline Beecham plc); Cpds. useful for treating allergic and inflammatory diseases. EP 0633776; EP 0919544; JP 1995508508; US 5552438; US 5602157; WO 9319749 .
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) 16510 3-(cyclopentyloxy)-4-methoxybenzaldehyde C13H16O3 详情 详情
(II) 16511 4-(bromomethyl)-2-(cyclopentyloxy)phenyl methyl ether; 4-(bromomethyl)-2-(cyclopentyloxy)-1-methoxybenzene C13H17BrO2 详情 详情
(III) 16512 2-[3-(cyclopentyloxy)-4-methoxyphenyl]acetonitrile C14H17NO2 详情 详情
(IV) 14156 methyl acrylate 96-33-3 C4H6O2 详情 详情
(V) 16514 dimethyl 4-cyano-4-[3-(cyclopentyloxy)-4-methoxyphenyl]heptanedioate C22H29NO6 详情 详情
(VI) 16515 methyl 5-cyano-5-[3-(cyclopentyloxy)-4-methoxyphenyl]-2-oxocyclohexanecarboxylate C21H25NO5 详情 详情
(VII) 16516 1-[3-(cyclopentyloxy)-4-methoxyphenyl]-4-oxocyclohexanecarbonitrile C19H23NO3 详情 详情
(VIII) 16517 1,3-dithian-2-yl(trimethyl)silane; 2-Trimethylsilyl-1,3-dithiane 13411-42-2 C7H16S2Si 详情 详情
(IX) 16518 1-[3-(cyclopentyloxy)-4-methoxyphenyl]-4-(1,3-dithian-2-ylidene)cyclohexanecarbonitrile C23H29NO2S2 详情 详情
(XII) 16519 methyl 4-cyano-4-[3-(cyclopentyloxy)-4-methoxyphenyl]cyclohexanecarboxylate C21H27NO4 详情 详情

合成路线2

The reaction of cyclohexanone (I) with chloroacetonitrile, KOH and benzyltriethylammonium chloride in THF gives the cyanoepoxide (II), which is treated with LiBr and LiOH in DMF/acetonitrile/water to yield the lithium salt (III) of the title product. Finally, this salt is treated with HCl in ethyl acetate to afford the target Cilomilast.

1 Badham, N.F.; Chen, J.-H.; Cummings, P.G.; Dell'Orco, P.C.; Diederich, A.M.; Eldridge, A.M.; Mendelson, W.L.; Mills, R.J.; Novack, V.J.; Olsen, M.A.; Rustum, A.M.; Webb, K.S.; Yang, S.; A practical synthesis of the PDE4 inhibitor, SB-207499, from a cyclohexanone precursor. Org Process Res Dev 2003, 7, 1, 101.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
31937 Triethylbenzylammonium chloride; N-benzyl-N,N-diethyl-1-ethanaminium chloride; Benzyltriethylammonium chloride 56-37-1 C13H22ClN 详情 详情
(I) 16516 1-[3-(cyclopentyloxy)-4-methoxyphenyl]-4-oxocyclohexanecarbonitrile C19H23NO3 详情 详情
(II) 61562 (2R)-6-[3-(cyclopentyloxy)-4-methoxyphenyl]-1-oxaspiro[2.5]octane-2,6-dicarbonitrile C21H24N2O3 详情 详情
(III) 61563 lithium 4-cyano-4-[3-(cyclopentyloxy)-4-methoxyphenyl]cyclohexanecarboxylate C20H24LiNO4 详情 详情
Extended Information