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【结 构 式】

【分子编号】54225

【品名】(4S,5R)-4,5-diphenyl-3-vinyl-1,3-oxazolidin-2-one

【CA登记号】n/a

【 分 子 式 】C17H15NO2

【 分 子 量 】265.31164

【元素组成】C 76.96% H 5.7% N 5.28% O 12.06%

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:(II)

The condensation of 6-chloropurine-2-amine (III) with the chiral monoacetate (II) (obtained by enzymatic desymmetrization of diacetate (I)) by means of Pd(PPh3)4 in DMSO gives the cyclopentenol derivative (IV), which is treated with dimethyl dicarbonate and DMAP in dichloromethane to yield the carbonate (V). The condensation of (V) with ethyl 2-nitroacetate (VI) by means of Pd in THF affords the adduct (VII), which is decarboxylated by means of NaCl in DMSO/water at 150 C to provide the nitromethylcyclopentene derivative (VIII). The reaction of (VIII) with tBuOK, O3 and NaBH4 in methanol gives the corresponding hydroxymethyl derivative (IX), which is finally hydrolyzed with NaOH in refluxing water to afford the target guanine as a racemic compound. Alternatively, the nitromethyl-cyclopentene derivative (VIII) can also be obtained by condensation of carbonate (V) with 2-(trimethylsilyl)ethyl 2-nitroacetate (X) by means of Pd in THF to give the adduct (XI), which is decarboxylated by means of CsF in hot acetonitrile, affording (VIII).

1 Brown, B.; Hegedus, L.S.; A novel, one pot ring expansion of cyclobutanones. Synthesis of carbovir and aristeromycin. J Org Chem 2000, 65, 6, 1865.
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) 54216   n/a C15H17CrO7 详情 详情
(II) 54225 (4S,5R)-4,5-diphenyl-3-vinyl-1,3-oxazolidin-2-one n/a C17H15NO2 详情 详情
(III) 54217 (4S,5R)-3-[(1S,2R)-2-(benzyloxy)-2-ethoxy-3-oxocyclobutyl]-4,5-diphenyl-1,3-oxazolidin-2-one n/a C28H27NO5 详情 详情
(IV) 54218 (4S,5R)-3-[(1S)-2-(benzyloxy)-4-oxo-2-cyclopenten-1-yl]-4,5-diphenyl-1,3-oxazolidin-2-one n/a C27H23NO4 详情 详情
(V) 54219 (4S,5R)-3-[(1S,2R)-2-(benzyloxy)-4-oxocyclopentyl]-4,5-diphenyl-1,3-oxazolidin-2-one n/a C27H25NO4 详情 详情
(VI) 54220 (4R)-4-(benzyloxy)-2-cyclopenten-1-one n/a C12H12O2 详情 详情
(VII) 54221 (1S,4R)-4-(benzyloxy)-2-cyclopenten-1-ol n/a C12H14O2 详情 详情
(VIII) 54222 (1S,4R)-4-(benzyloxy)-2-cyclopenten-1-yl ethyl carbonate n/a C15H18O4 详情 详情
(IX) 11644 6-Chloro-9H-purin-2-amine; 6-Chloro-9H-purin-2-ylamine; 2-Amino-6-chloropurine 10310-21-1 C5H4ClN5 详情 详情
(X) 54223 9-[(1S,4R)-4-(benzyloxy)-2-cyclopenten-1-yl]-6-chloro-9H-purin-2-amine; 9-[(1S,4R)-4-(benzyloxy)-2-cyclopenten-1-yl]-6-chloro-9H-purin-2-ylamine n/a C17H16ClN5O 详情 详情
(XI) 54224 (1R,4S)-4-(2-amino-6-chloro-9H-purin-9-yl)-2-cyclopenten-1-ol n/a C10H10ClN5O 详情 详情
Extended Information