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【结 构 式】

【分子编号】56639

【品名】4-methylene-1,2-cyclopentanedicarboxylic acid

【CA登记号】

【 分 子 式 】C8H10O4

【 分 子 量 】170.165

【元素组成】C 56.47% H 5.92% O 37.61%

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:(XIX)

Cyclization of the tetracarboxylic acid (XV) gives 4-oxocyclopentane-1,2-dicarboxylic acid (XVI), which is esterified with ethanol and sulfuric acid to yield the diester (XVII). Reaction of diester (XVII) with methyl-(triphenyl)phosphonium bromide and t-BuOK in THF affords 4-methylenecyclopentane-1,2-dicarboxylic acid diethyl ester (XVIII), which is hydrolyzed with KOH in THF/water to provide the corresponding free acid (XIX). The anhydrization of (XIX) by means of propionic anhydride at 135 C gives anhydride (III), which is submitted to an enantioselective quinine-mediated alcoholysis with 3-phenyl-2-propen-1-ol (XX) to yield (1R,2S)-2-amino-4-methylenecyclopentane-1-carboxylic acid 3-phenyl-2-propenyl monoester (XXI). Degradation of the free carboxylic acid group of (XXI) by means of DPPA, TEA and alcohol (XX) in hot toluene affords carbamate (XXII), which is finally fully deprotected with Pd(OAc)2 and PPh3 in ethanol.

1 Mittendorf, J.; Kunisch, F.; Matzke, M.; Militzer, H.-C.; Schmidt, A.; Schonfeld, W.; Novel antifungal beta-amino acids: Synthesis and activity against Candida albicans. Bioorg Med Chem Lett 2003, 13, 3, 433.
2 Sorbera, L.A.; Castañer, J.; Bozzo, J.; PLD-118. Drugs Fut 2002, 27, 11, 1049.
3 Schoenfeld, W.; Discovery, synthesis and SAR of beta-amino acid BAY 10-888/PLD-118, a novel antifungal for treatment of yeast infections. 42nd Intersci Conf Antimicrob Agents Chemother (Sept 27 2002, San Diego) 2002, Abst F-811.
4 Mittendorf, J. (Bayer AG); Efficient and highly enantioselective process for the preparation of enantiomerically pure cyclopentane-beta-amino acids . EP 0805145 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(III) 56629 (3aR,6aS)-5-methylenetetrahydro-1H-cyclopenta[c]furan-1,3(3aH)-dione C8H8O3 详情 详情
(XV) 56634 1,2,3,4-butanetetracarboxylic acid;1,2,3,4-Tetracarboxybutane 1703-58-8 C8H10O8 详情 详情
(XVI) 56635 4-oxo-1,2-cyclopentanedicarboxylic acid C7H8O5 详情 详情
(XVII) 56636 diethyl 4-oxo-1,2-cyclopentanedicarboxylate C11H16O5 详情 详情
(XVIII) 56638 diethyl 4-methylene-1,2-cyclopentanedicarboxylate C12H18O4 详情 详情
(XIX) 56639 4-methylene-1,2-cyclopentanedicarboxylic acid C8H10O4 详情 详情
(XX) 13951 (E)-3-Phenyl-2-propen-1-ol 104-54-1 C9H10O 详情 详情
(XXI) 27283 (1S,2R)-4-methylene-2-([[(E)-3-phenyl-2-propenyl]oxy]carbonyl)cyclopentanecarboxylic acid C17H18O4 详情 详情
(XXII) 56637 (E)-3-phenyl-2-propenyl (1R,2S)-4-methylene-2-{[({[(E)-3-phenyl-2-propenyl]oxy}carbonyl)amino]carbonyl}cyclopentanecarboxylate C27H27NO5 详情 详情
Extended Information