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【结 构 式】

【分子编号】62306

【品名】3-bromo[1,8]naphthyridine

【CA登记号】

【 分 子 式 】C8H5BrN2

【 分 子 量 】209.04518

【元素组成】C 45.97% H 2.41% Br 38.22% N 13.4%

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:(XXVI)

Elimination of the mesylate group of (XXIII) utilizing DBU in acetone leads to the 10,11-anhydro ketolide (XXIV). Acylation of (XXIV) with carbonyl diimidazole and NaH, followed by treatment with ammonium hydroxide gives rise to the 11,12-cyclic carbamate (XXV). Subsequent Heck coupling of allyl ether (XXV) with 3-bromo-1,8-naphthyridine (XXVI) leads to the (naphthyridinyl)propenyl derivative (XXVII). Then, fluorination of (XXVII) with N-fluorobenzenesulfonimide furnishes the 2-fluoro ketolide (XXVIII). Finally, the benzoate ester group of (XXVIII) is removed in refluxing MeOH to provide the title compound.

1 Macielag, M.; Abbanat, D.; Ashley, G.; Foleno, B.; Fu, H.; Li, Y.; Wira, E.; Bush, K.; Structure-activity studies of 15-methyl ketolides: Optimization of the heterocyclic substituent. 42nd Intersci Conf Antimicrob Agents Chemother (Sept 27 2002, San Diego) 2002, Abst F-1662.
2 Hlasta, D.; Khosla, C.; Chu, D.T.W.; Ashley, G.; Henninger, T.C.; Grant, E.B. (Ortho-McNeil Pharmaceutical, Inc.); Ketolide antibacterials. WO 0232918 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(XXIII) 62303 (2S,3R,4S,6R)-2-({(3R,5R,6R,7S,9R,11R,12R,13R,14R)-7-(allyloxy)-13-hydroxy-3,5,7,9,11,13-hexamethyl-12-[(methylsulfonyl)oxy]-2,4,10-trioxo-14-propyloxacyclotetradecanyl}oxy)-4-(dimethylamino)-6-methyltetrahydro-2H-pyran-3-yl benzoate C41H63NO13S 详情 详情
(XXIV) 62304 (2S,3R,4S,6R)-2-{[(3R,5R,6R,7S,9R,13S,14R)-7-(allyloxy)-13-hydroxy-3,5,7,9,11,13-hexamethyl-2,4,10-trioxo-14-propyloxa-11-cyclotetradecen-6-yl]oxy}-4-(dimethylamino)-6-methyltetrahydro-2H-pyran-3-yl benzoate C40H59NO10 详情 详情
(XXV) 62305 (2S,3R,4S,6R)-2-{[(3aS,4R,7R,9R,10R,11S,13R,15R,15aR)-11-(allyloxy)-3a,7,9,11,13,15-hexamethyl-2,6,8,14-tetraoxo-4-propyltetradecahydro-2H-oxacyclotetradecino[4,3-d][1,3]oxazol-10-yl]oxy}-4-(dimethylamino)-6-methyltetrahydro-2H-pyran-3-yl benzoate C41H60N2O11 详情 详情
(XXVI) 62306 3-bromo[1,8]naphthyridine C8H5BrN2 详情 详情
(XXVII) 62307 (2S,3R,4S,6R)-2-[((3aS,4R,7R,9R,10R,11S,13R,15R,15aR)-3a,7,9,11,13,15-hexamethyl-11-{[(E)-3-[1,8]naphthyridin-3-yl-2-propenyl]oxy}-2,6,8,14-tetraoxo-4-propyltetradecahydro-2H-oxacyclotetradecino[4,3-d][1,3]oxazol-10-yl)oxy]-4-(dimethylamino)-6-methy C49H64N4O11 详情 详情
(XXVIII) 62308 (2S,3R,4S,6R)-2-[((3aS,4R,7S,9R,10R,11S,13R,15R,15aR)-7-fluoro-3a,7,9,11,13,15-hexamethyl-11-{[(E)-3-[1,8]naphthyridin-3-yl-2-propenyl]oxy}-2,6,8,14-tetraoxo-4-propyltetradecahydro-2H-oxacyclotetradecino[4,3-d][1,3]oxazol-10-yl)oxy]-4-(dimethylamino C49H63FN4O11 详情 详情
Extended Information