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【结 构 式】

【分子编号】43605

【品名】methyl (4S,5S)-4-[(1S,2S)-1-hydroxy-2-methyl-3-butenyl]-5-isopropyl-2-phenyl-4,5-dihydro-1,3-oxazole-4-carboxylate

【CA登记号】

【 分 子 式 】C19H25NO4

【 分 子 量 】331.41184

【元素组成】C 68.86% H 7.6% N 4.23% O 19.31%

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:(XXV)

Sharpless epoxidation of (XIII) with cumene hydroperoxide, diisopropyl L-tartrate ((+)-DIPT) and Ti(O-i-Pr)4 affords epoxide (-)-(XIV), which is then treated with benzyl isocyanate and NaH in refluxing THF to yield oxazolidinone (XV). Oxidation of (XV) by means of CrO3 in H2SO4 (Jones reagent) in acetone gives the corresponding carboxylic acid (XVI), which is converted into methyl ester (XVII) via diazomethane esterification in Et2O. Exposure of (XVII) to ethanolic KOH affords the trans-acid (XVIII), which is then converted into (2R,3S)-hydroxyleucine (XIX) by treatment with KOH and hydrogenolysis over Pd(OH)2 in MeOH. Esterification of (XIX) by means of MeOH and HCl (gas) provides (XX), which is treated with methyl benzimidate (Ph(MeO)C=NH) or methyl orthobenzoate (PhC(OMe)3) in the presence of catalytic p-TsOH to yield trans-oxazoline (XXI). Aldol condensation of (XXI) with formaldehyde and LHMDS via the Seebach protocol gives (XXII), which is converted into (XXIII) via Moffat oxidation with DCC and TFA in benzene/DMSO. Brown asymmetric allylboration of (XIII) in THF with (E)-crotyl(diisopinocampheyl)borane (XXIV) in Et2O affords a homoallylic alcohol mixture from which diastereomer (-)-(XXV) is obtained. Ozonolysis of (-)-(XXV) and reductive treatment with dimethylsulfide (DMS), followed by oxidation with NaClO2, NaH2PO4 and 2-methyl-2-butene, provides carboxylic acid (XXVI), which is then converted into (X) by means of Pd and HCOONH4 in refluxing HOAc followed by saponification with NaOH. Lactam ester derivative (X) reacts with N-acetyl-L-cysteine allyl ester (XXVII), BOPCl and Et3N in CH2Cl2 to furnish (XVIII), which is finally deallylated by means of Pd(PPh3)4, HCO2H and Et3N in THF.

1 Sunazuka, T.; et al.; Total synthesis of (+)-lactacystin, the first non-protein neurotrophic factor. J Am Chem Soc 1993, 115, 5302.
2 Nagamitsu, T.; et al.; Total synthesis of (+)-lactacystin. J Am Chem Soc 1996, 118, 15, 3584.
3 Corey, E.J.; Li, W.-D.Z.; Total synthesis and biological activity of lactacystin, omuralide and analogs. Chem Pharm Bull 1999, 47, 1, 1.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(X) 43607 (2S,3S,4R)-3-hydroxy-2-[(1S)-1-hydroxy-2-methylpropyl]-4-methyl-5-oxo-2-pyrrolidinecarboxylic acid C10H17NO5 详情 详情
(XIII) 43593 (E)-4-methyl-2-penten-1-ol C6H12O 详情 详情
(XIV) 43594 [(2R,3S)-3-isopropyloxiranyl]methanol C6H12O2 详情 详情
(XV) 43595 (4R,5S)-3-benzyl-4-(hydroxymethyl)-5-isopropyl-1,3-oxazolidin-2-one C14H19NO3 详情 详情
(XVI) 43596 (4S,5S)-3-benzyl-5-isopropyl-2-oxo-1,3-oxazolidine-4-carboxylic acid C14H17NO4 详情 详情
(XVII) 43597 methyl (4S,5S)-3-benzyl-5-isopropyl-2-oxo-1,3-oxazolidine-4-carboxylate C15H19NO4 详情 详情
(XVIII) 43598 (4R,5S)-3-benzyl-5-isopropyl-2-oxo-1,3-oxazolidine-4-carboxylic acid C14H17NO4 详情 详情
(XIX) 43599 (2R,3S)-2-amino-3-hydroxy-4-methylpentanoic acid C6H13NO3 详情 详情
(XX) 43600 methyl (2R,3S)-2-amino-3-hydroxy-4-methylpentanoate C7H15NO3 详情 详情
(XXI) 43601 (4S,5S)-5-isopropyl-4-methyl-2-phenyl-4,5-dihydro-1,3-oxazole C13H17NO 详情 详情
(XXII) 43602 methyl (4S,5S)-4-(hydroxymethyl)-5-isopropyl-2-phenyl-4,5-dihydro-1,3-oxazole-4-carboxylate C15H19NO4 详情 详情
(XXIII) 43603 methyl (4R,5S)-4-formyl-5-isopropyl-2-phenyl-4,5-dihydro-1,3-oxazole-4-carboxylate C15H17NO4 详情 详情
(XXIV) 43604 (E)-2-butenyl[bis[(1S,2R,3S,5S)-1,2,5,6,6-pentamethylbicyclo[3.1.1]hept-3-yl]]borane C28H49B 详情 详情
(XXV) 43605 methyl (4S,5S)-4-[(1S,2S)-1-hydroxy-2-methyl-3-butenyl]-5-isopropyl-2-phenyl-4,5-dihydro-1,3-oxazole-4-carboxylate C19H25NO4 详情 详情
(XXVI) 43606 (2R,3S)-3-hydroxy-3-[(4S,5S)-5-isopropyl-4-(methoxycarbonyl)-2-phenyl-4,5-dihydro-1,3-oxazol-4-yl]-2-methylpropionic acid C18H23NO6 详情 详情
(XXVII) 43608 allyl (2R)-2-(acetamido)-3-sulfanylpropanoate C8H13NO3S 详情 详情
(XXVIII) 43609 allyl (2R)-2-(acetamido)-3-[([(2S,3S,4R)-3-hydroxy-2-[(1S)-1-hydroxy-2-methylpropyl]-4-methyl-5-oxopyrrolidinyl]carbonyl)sulfanyl]propanoate C18H28N2O7S 详情 详情
Extended Information