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【结 构 式】

【药物名称】

【化学名称】2(S)-(Benzyloxycarbonylamino)-3-[2-[4(S)-[3-(4,5-dihydro-1H-imidazol-2-ylamino)propyl]-2,5-dioxoimidazolidin-1-yl]acetamido]propionic acid

【CA登记号】

【 分 子 式 】C22H29N7O7

【 分 子 量 】503.51913

【开发单位】Aventis Pharma (Originator)

【药理作用】Bone Diseases, Treatment of, Bone Resorption Inhibitors, METABOLIC DRUGS, Treatment of Osteoporosis, Integrin alphavbeta3 (Vitronectin) Antagonists

合成路线1

Conversion of amino acid (I) into its methyl ester derivative (II) by means of SOCl2 in MeOH, followed by coupling with ethyl isocyanatoacetate (III) and Et3N in CH2Cl2/THF yields derivative (IV). Cyclization of (IV) by means of H2O/HCl affords hydantoin (V), which reacts with 2-methylthio-2-imidazoline (VI) in an aqueous NaOH solution to provide cyclic guanidine derivative (VII). Treatment of amino acid (VIII) with isobutylene (IX) and H2SO4 in dioxane affords t-Bu ester (X), which then couples with (VII) by means of HOBt and DCC in DMF to furnish derivative (XI). Finally, tert-butyl ester is hydrolyzed by treatment with TFA in the presence of 1,2-dimercaptoethane.

1 Knolle, J.; Peyman, A.; Wehner, V.; et al.; RGD mimetics containing a central hydantoin scaffold: alphavbeta3 vs alphaIIbbeta3 selective requirements. Bioorg Med Chem Lett 2000, 10, 2, 179.
2 Wehner, V.; Knolle, J.; Stilz, H.U.; Carniato, D.; Gourvest, J.-F.; Gadek, T.; McDowell, R. (Aventis SA); Inhibitors of bone resorption and vitronectin receptor antagonists. DE 19626701; DE 19635522; EP 0796855 .
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) 30898 (2S)-2-amino-5-[[(benzyloxy)carbonyl]amino]pentanoic acid C13H18N2O4 详情 详情
(II) 42993 methyl (2S)-2-amino-5-[[(benzyloxy)carbonyl]amino]pentanoate C14H20N2O4 详情 详情
(III) 18312 ETHYL ISOCYANATOACETATE; ethyl 2-isocyanatoacetate 2949-22-6 C5H7NO3 详情 详情
(IV) 42994 12-ethyl 8-methyl (8S)-3,10-dioxo-1-phenyl-2-oxa-4,9,11-triazadodecane-8,12-dicarboxylate C19H27N3O7 详情 详情
(V) 42295 (2R)-N-methyl-2-(methylamino)-3-(2-naphthyl)-N-[(1R)-2-oxo-1-(2-thienylmethyl)-2-(1,2,2-trimethylhydrazino)ethyl]propanamide C25H32N4O2S 详情 详情
(VI) 42996 4,5-dihydro-1H-imidazol-2-yl methyl sulfide; 2-(methylsulfanyl)-4,5-dihydro-1H-imidazole 5464-11-9 C4H8N2S 详情 详情
(VII) 42997 2-[(4S)-4-[3-(4,5-dihydro-1H-imidazol-2-ylamino)propyl]-2,5-dioxoimidazolidinyl]acetic acid C11H17N5O4 详情 详情
(VIII) 18008 (2S)-3-amino-2-[[(benzyloxy)carbonyl]amino]propionic acid; N(alpha)-Z-L-2,3-diaminopropionic acid 35761-26-3 C11H14N2O4 详情 详情
(IX) 15926 2-methyl-1-propene; isobutylene 115-11-7 C4H8 详情 详情
(X) 18009 tert-butyl (2S)-3-amino-2-[[(benzyloxy)carbonyl]amino]propanoate C15H22N2O4 详情 详情
(XI) 42998 tert-butyl (2S)-2-[[(benzyloxy)carbonyl]amino]-3-[(2-[(4S)-4-[3-(4,5-dihydro-1H-imidazol-2-ylamino)propyl]-2,5-dioxoimidazolidinyl]acetyl)amino]propanoate C26H37N7O7 详情 详情
Extended Information