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【结 构 式】 
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【分子编号】38157 【品名】(2S,3R,4S,6R)-2-[[(3aS,4R,7R,8S,9R,10R,11R,13R,15R,15aR)-1-(4-chlorophenethyl)-4-ethyl-11-methoxy-8-([(4R,5S,6S)-4-methoxy-4,6-dimethyl-5-[(trimethylsilyl)oxy]tetrahydro-2H-pyran-2-yl]oxy)-3a,7,9,11,13,15-hexamethyl-2,6,14-trioxotetradecahydro-2H-oxacyclotetradecino[4,3-d][1,3]oxazol-10-yl]oxy]-4-(dimethylamino)-6-methyltetrahydro-2H-pyran-3-yl acetate 【CA登记号】 |
【 分 子 式 】C52H85ClN2O14Si 【 分 子 量 】1025.79018 【元素组成】C 60.89% H 8.35% Cl 3.46% N 2.73% O 21.84% Si 2.74% |
合成路线1
该中间体在本合成路线中的序号：(V)Protection of 2'-O-acetyl-6-O-methylerythromycin A (I) with chlorotrimethylsilane afforded the 4''-O-trimethylsilyl derivative (II). Subsequent treatment with carbonyldiimidazole and NaH produced the dehydrated imidazolide (III), which was converted to the cyclic carbamate (V) upon reaction with 4-chlorophenethyl amine (IV). Acid hydrolysis of the cladinose moiety gave alcohol (VI), and further condensation with carbonyldiimidazole yielded imidazolide (VII).
| 【1】 Waid, P.; Dalton, C.R.; Randolph, J.T.; Greer, J.; Nichols, C.J.; Haviv, F.; Mort, N.A.; Sauer, D.R. (Abbott Laboratories Inc.); Macrolide LHRH antagonists. WO 0012522 . |
| 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) | 38154 | (2S,3R,4S,6R)-4-(dimethylamino)-2-[((3R,4S,5R,6R,7R,9R,11R,12R,13S,14R)-14-ethyl-12,13-dihydroxy-4-[[(4R,5S,6S)-5-hydroxy-4-methoxy-4,6-dimethyltetrahydro-2H-pyran-2-yl]oxy]-7-methoxy-3,5,7,9,11,13-hexamethyl-2,10-dioxooxacyclotetradecanyl)oxy]-6-methyltetrahydro-2H-pyran-3-yl acetate | C40H71NO14 | 详情 | 详情 | |
| (II) | 38155 | (2S,3R,4S,6R)-4-(dimethylamino)-2-[[(3R,4S,5R,6R,7R,9R,11R,12R,13S,14R)-14-ethyl-12,13-dihydroxy-7-methoxy-4-([(4R,5S,6S)-4-methoxy-4,6-dimethyl-5-[(trimethylsilyl)oxy]tetrahydro-2H-pyran-2-yl]oxy)-3,5,7,9,11,13-hexamethyl-2,10-dioxooxacyclotetradecanyl]oxy]-6-methyltetrahydro-2H-pyran-3-yl acetate | C43H79NO14Si | 详情 | 详情 | |
| (III) | 38156 | (2R,3S,7R,9R,10R,11R,12S,13R)-10-[[(2S,3R,4S,6R)-3-(acetoxy)-4-(dimethylamino)-6-methyltetrahydro-2H-pyran-2-yl]oxy]-2-ethyl-9-methoxy-12-([(4R,5S,6S)-4-methoxy-4,6-dimethyl-5-[(trimethylsilyl)oxy]tetrahydro-2H-pyran-2-yl]oxy)-3,5,7,9,11,13-hexamethyl-6,14-dioxooxa-4-cyclotetradecen-3-yl 1H-imidazole-1-carboxylate | C47H79N3O14Si | 详情 | 详情 | |
| (IV) | 29459 | 4-chlorophenethylamine; 2-(4-chlorophenyl)-1-ethanamine | 156-41-2 | C8H10ClN | 详情 | 详情 |
| (V) | 38157 | (2S,3R,4S,6R)-2-[[(3aS,4R,7R,8S,9R,10R,11R,13R,15R,15aR)-1-(4-chlorophenethyl)-4-ethyl-11-methoxy-8-([(4R,5S,6S)-4-methoxy-4,6-dimethyl-5-[(trimethylsilyl)oxy]tetrahydro-2H-pyran-2-yl]oxy)-3a,7,9,11,13,15-hexamethyl-2,6,14-trioxotetradecahydro-2H-oxacyclotetradecino[4,3-d][1,3]oxazol-10-yl]oxy]-4-(dimethylamino)-6-methyltetrahydro-2H-pyran-3-yl acetate | C52H85ClN2O14Si | 详情 | 详情 | |
| (VI) | 38158 | (2S,3R,4S,6R)-2-[[(3aS,4R,7R,8S,9S,10R,11R,13R,15R,15aR)-1-(4-chlorophenethyl)-4-ethyl-8-hydroxy-11-methoxy-3a,7,9,11,13,15-hexamethyl-2,6,14-trioxotetradecahydro-2H-oxacyclotetradecino[4,3-d][1,3]oxazol-10-yl]oxy]-4-(dimethylamino)-6-methyltetrahydro-2H-pyran-3-yl acetate | C41H63ClN2O11 | 详情 | 详情 | |
| (VII) | 38159 | (3aS,4R,7R,8S,9R,10R,11R,13R,15R,15aR)-10-[[(2S,3R,4S,6R)-3-(acetoxy)-4-(dimethylamino)-6-methyltetrahydro-2H-pyran-2-yl]oxy]-1-(4-chlorophenethyl)-4-ethyl-11-methoxy-3a,7,9,11,13,15-hexamethyl-2,6,14-trioxotetradecahydro-2H-oxacyclotetradecino[4,3-d][1,3]oxazol-8-yl 1H-imidazole-1-carboxylate | C45H65ClN4O12 | 详情 | 详情 |