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【结 构 式】

【分子编号】63276

【品名】benzyl (2S)-3-iodo-2-(tritylamino)propanoate

【CA登记号】

【 分 子 式 】C29H26INO2

【 分 子 量 】547.43545

【元素组成】C 63.63% H 4.79% I 23.18% N 2.56% O 5.85%

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:(XI)

Treatment of N-trityl-D-serine benzyl ester (X) with I2/PPh3 gives rise to the iodoalanine derivative (XI). Thiol (IX) is then alkylated by iodide (XI) in the presence of Cs2CO3 to furnish thioether (XII). Simultaneous cleavage from the resin and removal of the N-trityl group in (XII) employing trifluoroacetic acid leads to the linear pentapeptide derivative (XIII). This is then cyclized to (XIV) in the presence of DPPA and NaHCO3 in dilute DMF solution. The Cbz and benzyl protecting groups of (XIV) are finally removed by HBr in AcOH to provide the title compound.

1 Rew, Y.; Malkmus, S.; Svensson, C.; Yaksh, T.L.; Chung, N.N.; Schiller, P.W.; Cassel, J.A.; DeHaven, R.; Goodman, M.; Synthesis and biological activities of cyclic lanthionine enkephalin analogues: delta-Opioid receptor selective ligands. J Med Chem 2002, 45, 17, 3746.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(IX) 63274 (5S,8S,14S)-14-benzyl-5-[4-(benzyloxy)benzyl]-8-(1-methyl-1-sulfanylethyl)-3,6,9,12-tetraoxo-1-phenyl-2-oxa-4,7,10,13-tetraazapentadecan-15-oic acid C40H44N4O8S 详情 详情
(X) 63275 benzyl (2R)-3-hydroxy-2-(tritylamino)propanoate C29H27NO3 详情 详情
(XI) 63276 benzyl (2S)-3-iodo-2-(tritylamino)propanoate C29H26INO2 详情 详情
(XII) 63277 (5S,8S,14S)-14-benzyl-5-[4-(benzyloxy)benzyl]-8-(1-{[(2S)-3-(benzyloxy)-3-oxo-2-(tritylamino)propyl]sulfanyl}-1-methylethyl)-3,6,9,12-tetraoxo-1-phenyl-2-oxa-4,7,10,13-tetraazapentadecan-15-oic acid C69H69N5O10S 详情 详情
(XIII) 63278 (5S,8S,14S)-8-(1-{[(2S)-2-amino-3-(benzyloxy)-3-oxopropyl]sulfanyl}-1-methylethyl)-14-benzyl-5-[4-(benzyloxy)benzyl]-3,6,9,12-tetraoxo-1-phenyl-2-oxa-4,7,10,13-tetraazapentadecan-15-oic acid C50H55N5O10S 详情 详情
(XIV) 63279 benzyl (3S,6S,12S)-6-benzyl-12-({(2S)-2-{[(benzyloxy)carbonyl]amino}-3-[4-(benzyloxy)phenyl]propanoyl}amino)-13,13-dimethyl-5,8,11-trioxo-1-thia-4,7,10-triazacyclotridecane-3-carboxylate C50H53N5O9S 详情 详情
Extended Information