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【结 构 式】

【分子编号】47263

【品名】(2S)-2-(dibenzylamino)-1-propanol

【CA登记号】

【 分 子 式 】C17H21NO

【 分 子 量 】255.35988

【元素组成】C 79.96% H 8.29% N 5.49% O 6.27%

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:(III)

Alanine methyl ester (I) was protected by N-alkylation with benzyl bromide to afford (II), which was further reduced to amino alcohol (III) using LiAlH4. Swern oxidation of (III) provided aldehyde (IV). Addition of the Grignard reagent obtained from 1-bromopentadecane (A) to aldehyde (IV) produced the anti-aminoalcohol (V). The N-benzyl groups were finally removed by catalytic hydrogenolysis.

1 Cuadros, R.; et al.; The marine compound spisulosine, an inhibitor of cell proliferation, promotes the disassembly of actin stress fibers. Cancer Letters 2000, 152, 1, 23.
2 Garcia Gravalos, D.; Warwick, R.A.; Avila, J.; Rinehart, K.L.; Fregeau, N.L.; Faircloth, G.T. (University of Illinois); Spisulosine cpds. having antitumour activity. WO 9952521 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(A) 47265 bromo(tetradecyl)magnesium C14H29BrMg 详情 详情
(I) 20694 methyl (2S)-2-aminopropanoate C4H9NO2 详情 详情
(II) 47262 methyl (2S)-2-(dibenzylamino)propanoate C18H21NO2 详情 详情
(III) 47263 (2S)-2-(dibenzylamino)-1-propanol C17H21NO 详情 详情
(IV) 47264 (2S)-2-(dibenzylamino)propanal C17H19NO 详情 详情
(V) 47266 (2S,3R)-2-(dibenzylamino)-3-octadecanol C32H51NO 详情 详情
Extended Information