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【结 构 式】

【分子编号】32863

【品名】ethyl 2-[[(benzyloxy)carbonyl]amino]-2-cyanoacetate

【CA登记号】

【 分 子 式 】C13H14N2O4

【 分 子 量 】262.26524

【元素组成】C 59.54% H 5.38% N 10.68% O 24.4%

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:(I)

The alkylation of ethyl 2-(benzyloxycarbonylamino)cyanoacetate (I) with ethyl bromoacetate and anhydrous potassium carbonate in acetone gives diethyl 2-(benzyloxycarbonylamino)-2-cyanosuccinate (II), which is hydrolyzed by means of hydrogen peroxide and sodium carbonate in acetone/water, yielding 3-(benzyloxycarbonylamino)-3-(ethoxycarbonyl)pyrrolidine-2,5-dione (III). Racemic (III) is then resolved by means of crystallization with cinchonidine in ethanol to give the (-)-enantiomer (IV) (>99.5% e.e.). Hydrogenolysis of (IV) over Pd/C in ethanol, followed by treatment with 2,5-dimethoxytetrahydrofuran in acetic acid, affords (-)-3-(ethoxycarbonyl)-3-(pyrrol-1-yl)pyrrolidine-2,5-dione (VI). Treatment of (VI) with trichloroacetyl chloride in ethyl acetate, followed by condensation with 4-bromo-2-fluorobenzylamine in the presence of triethylamine, gives AS-3201 (>99.4% e.e.).

1 Negoro, T.; Murata, M.; Ueda, S.; Fujitani, B.; Ono, Y.; Kuromiya, A.; Komiya, M.; Suzuki, M.; Matsumoto, J.; Novel, highly potent aldose reductase inhibitors: (R)-(-)-2-(4-Bromo-2-fluorobenzyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine-4-spiro-3'-pyrrolidine-1,2',3,5'-tetrone (AS-3201) and its congeners. J Med Chem 1998, 41, 21, 4118-29.
2 Negoro, T.; Komiya, M.; Ono, Y.; AS-3201. Drugs Fut 2000, 25, 2, 131.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
12132 2,5-Dimethoxytetrahydrofuran; 5-Methoxytetrahydro-2-furanyl methyl ether 696-59-3 C6H12O3 详情 详情
16640 Ethyl 2-bromoacetate; Ethyl bromoacetate 105-36-2 C4H7BrO2 详情 详情
19560 (4-bromo-2-fluorophenyl)methanamine; 4-bromo-2-fluorobenzylamine 112734-22-2 C7H7BrFN 详情 详情
(I) 32863 ethyl 2-[[(benzyloxy)carbonyl]amino]-2-cyanoacetate C13H14N2O4 详情 详情
(II) 32864 diethyl 2-[[(benzyloxy)carbonyl]amino]-2-cyanosuccinate C17H20N2O6 详情 详情
(III) 32865 ethyl 3-[[(benzyloxy)carbonyl]amino]-2,5-dioxo-3-pyrrolidinecarboxylate C15H16N2O6 详情 详情
(IV) 32866 ethyl (3R)-3-[[(benzyloxy)carbonyl]amino]-2,5-dioxo-3-pyrrolidinecarboxylate C15H16N2O6 详情 详情
(V) 32867 ethyl (3R)-3-amino-2,5-dioxo-3-pyrrolidinecarboxylate C7H10N2O4 详情 详情
(VI) 32868 ethyl (3R)-2,5-dioxo-3-(1H-pyrrol-1-yl)-3-pyrrolidinecarboxylate C11H12N2O4 详情 详情
(VII) 32869 ethyl (3R)-2,5-dioxo-3-[2-(2,2,2-trichloroacetyl)-1H-pyrrol-1-yl]-3-pyrrolidinecarboxylate C13H11Cl3N2O5 详情 详情
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