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【结 构 式】

【分子编号】50951

【品名】2-(3-fluoroanilino)acetamide

【CA登记号】

【 分 子 式 】C8H9FN2O

【 分 子 量 】168.1707432

【元素组成】C 57.14% H 5.39% F 11.3% N 16.66% O 9.51%

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)

The alkylation of 3-fluoroaniline (I) with 2-bromoacetamide (II) by means of KOH and Bu4NBr in THF gives 2-(3-fluorophenylamino)acetamide (III), which is condensed with 4-acetoxy-3,6-dihydro-2H-pyran-2,6-dione (IV) in Ac-OH to yield intermediate (V). The cyclization of (V) by means of H2SO4 or Ms-OH at 100?C affords the quinolone (VII), which is esterified with SOCl2 and methanol to provide the corresponding methyl ester (VII). The reduction of (VII) with NaBH4 in refluxing THF furnishes the 2-hydroxyethyl quinolone (VIII), which is treated with SOCl2 in refluxing CHCl3 to give the 2-chloroethyl derivative (IX). Finally, this compound is condensed with the arylpiperazine (X) by means of K2CO3 and KI in hot DMF to afford the desired quinolone.

1 McCort, G.; et al.; Synthesis and SAR of 3- and 4-substituted quinolin-2-ones: Discovery of mixed 5-HT1b/5-HT2A receptor antagonists. Bioorg Med Chem 2001, 9, 8, 2129.
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) 20697 3-fluoroaniline; 3-fluorophenylamine 372-19-0 C6H6FN 详情 详情
(II) 38747 2-bromoacetamide 683-57-8 C2H4BrNO 详情 详情
(III) 50951 2-(3-fluoroanilino)acetamide C8H9FN2O 详情 详情
(IV) 40692 2,6-dioxo-3,6-dihydro-2H-pyran-4-yl acetate C7H6O5 详情 详情
(V) 50952 (Z)-3-(acetoxy)-5-[(2-amino-2-oxoethyl)-3-fluoroanilino]-5-oxo-2-pentenoic acid C15H15FN2O6 详情 详情
(VI) 50953 2-[1-(2-amino-2-oxoethyl)-7-fluoro-2-oxo-1,2-dihydro-4-quinolinyl]acetic acid C13H11FN2O4 详情 详情
(VII) 50954 methyl 2-[1-(2-amino-2-oxoethyl)-7-fluoro-2-oxo-1,2-dihydro-4-quinolinyl]acetate C14H13FN2O4 详情 详情
(VIII) 50955 2-[7-fluoro-4-(2-hydroxyethyl)-2-oxo-1(2H)-quinolinyl]acetamide C13H13FN2O3 详情 详情
(IX) 50956 2-[4-(2-chloroethyl)-7-fluoro-2-oxo-1(2H)-quinolinyl]acetamide C13H12ClFN2O2 详情 详情
(X) 40698 4-(1-piperazinyl)thieno[3,2-c]pyridine C11H13N3S 详情 详情
Extended Information