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【结 构 式】

【分子编号】50783

【品名】2,2,2-trichloroethyl (3S,4R,5S)-4-[[(2S,3R)-2-amino-3-(benzyloxy)butanoyl]amino]-3-hydroxy-5-methylheptanoate

【CA登记号】

【 分 子 式 】C21H31Cl3N2O5

【 分 子 量 】497.84572

【元素组成】C 50.66% H 6.28% Cl 21.36% N 5.63% O 16.07%

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:(X)

Protection of the carboxyl group of Boc-L-threonine (I) with [2-(chloromethoxy)ethyl]trimethylsilane (SEM-Cl) (II) by means of Li2CO3 affords protected threonine (III). Separately, Z-L-tyrosine (IV) is treated with dimethyl sulfate and KOH in THF with tetrabutylammonium hydrogen sulfate as a catalyst to furnish N,O-dimethyl-L-tyrosine (V), which is then converted into secondary amine (VI) by coupling with protected threonine (III) either by means of 2,4,6-trichlorobenzoyl chloride in THF and DMAP in benzene or with isopropenyl chloroformate, Et3N and DMAP, followed by elimination of the carbobenzyloxy group by hydrogenation over Pd/C. Coupling of Z-L-leucine (IX) to L-proline methyl ester (X) by means of DCC, HOBt and NMM in CH2Cl2, followed by hydrolysis with LiOH, affords Z-leucylproline (VII), which is then coupled to amine (VI) by means of BOPCl and Et3N in CH2Cl2, and then subjected to deprotection with hydrofluoric acid in acetonitrile affording intermediate (VIII).

1 Hamada, Y.; Shioiri, T.; Anti-tumor active cyclic peptide derived from marine organism: Synthesis, conformation and bioactivity. Kagaku Zokan 1990, 118, 31.
2 Harris, B.D.; et al.; Synthetic studies of didemnins. II. Approaches to statine diastereomers. Tetrahedron Lett 1987, 28, 25, 2837.
3 Hamada, Y.; et al.; Efficient total synthesis of didemnins A and B. J Am Chem Soc 1989, 111, 2, 669.
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) 50775 (2R,3S)-2-[(tert-butoxycarbonyl)amino]-3-methylpentanoic acid C11H21NO4 详情 详情
(II) 44205 (2-ethoxy-2-oxoethyl)lithium C4H7LiO2 详情 详情
(III) 50776 ethyl (4R,5S)-4-[(tert-butoxycarbonyl)amino]-5-methyl-3-oxoheptanoate C15H27NO5 详情 详情
(IV) 50777 tert-butyl (1R,2S)-1-formyl-2-methylbutylcarbamate C11H21NO3 详情 详情
(V) 50778 ethyl (3S,4R,5S)-4-[(tert-butoxycarbonyl)amino]-3-hydroxy-5-methylheptanoate C15H29NO5 详情 详情
(VI) 50779 2,2,2-trichloro-1-ethanol C2H3Cl3O 详情 详情
(VII) 50780 2,2,2-trichloroethyl (3S,4R,5S)-4-[(tert-butoxycarbonyl)amino]-3-hydroxy-5-methylheptanoate C15H26Cl3NO5 详情 详情
(VIII) 50781 2,2,2-trichloroethyl (3S,4R,5S)-4-amino-3-hydroxy-5-methylheptanoate C10H18Cl3NO3 详情 详情
(IX) 50782 (2S,3R)-3-(benzyloxy)-2-[(tert-butoxycarbonyl)amino]butyric acid C16H23NO5 详情 详情
(X) 50783 2,2,2-trichloroethyl (3S,4R,5S)-4-[[(2S,3R)-2-amino-3-(benzyloxy)butanoyl]amino]-3-hydroxy-5-methylheptanoate C21H31Cl3N2O5 详情 详情
(XI) 50788 (2R)-2-[(tert-butoxycarbonyl)(methyl)amino]-4-methylpentanoic acid C12H23NO4 详情 详情
(XII) 31819 (2R)-2-[(tert-butoxycarbonyl)amino]-4-methylpentanoic acid 16937-99-8 C11H21NO4 详情 详情
(XIII) 50787 2,2,2-trichloroethyl (6R,9S,12R,13S)-9-[(1R)-1-(benzyloxy)ethyl]-13-[[tert-butyl(dimethyl)silyl]oxy]-6-isobutyl-2,2,5-trimethyl-12-[(1S)-1-methylpropyl]-4,7,10-trioxo-3-oxa-5,8,11-triazapentadecan-15-oate C39H66Cl3N3O8Si 详情 详情
(XIV) 50784 2,2,2-trichloroethyl (6R,9S,12R,13S)-13-[[tert-butyl(dimethyl)silyl]oxy]-9-[(1R)-1-hydroxyethyl]-6-isobutyl-2,2,5-trimethyl-12-[(1S)-1-methylpropyl]-4,7,10-trioxo-3-oxa-5,8,11-triazapentadecan-15-oate C32H60Cl3N3O8Si 详情 详情
(XV) 50747 (2S)-2-[[(benzyloxy)carbonyl](methyl)amino]-3-(4-methoxyphenyl)propionic acid C19H21NO5 详情 详情
(XVI) 39328 (2S)-2-[[(benzyloxy)carbonyl]amino]-3-(4-hydroxyphenyl)propionic acid C17H17NO5 详情 详情
(XVII) 50785 2,2,2-trichloroethyl (5S,8R,9S,12R,13S)-13-[[tert-butyl(dimethyl)silyl]oxy]-5-(4-methoxybenzyl)-4,8-dimethyl-9-[[(2R)-4-methyl-2-(methylamino)pentanoyl]amino]-12-[(1S)-1-methylpropyl]-3,6,10-trioxo-1-phenyl-2,7-dioxa-4,11-diazapentadecan-15-oate C46H71Cl3N4O10Si 详情 详情
(XVIII) 50786 (5S,8R,9S,12R,13S)-13-[[tert-butyl(dimethyl)silyl]oxy]-5-(4-methoxybenzyl)-4,8-dimethyl-9-[[(2R)-4-methyl-2-(methylamino)pentanoyl]amino]-12-[(1S)-1-methylpropyl]-3,6,10-trioxo-1-phenyl-2,7-dioxa-4,11-diazapentadecan-15-oic acid C44H70N4O10Si 详情 详情
Extended Information