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【结 构 式】

【分子编号】19903

【品名】ethyl 6-fluoro-4-oxo-1,4-dihydro-3-quinolinecarboxylate

【CA登记号】

【 分 子 式 】C12H10FNO3

【 分 子 量 】235.2147432

【元素组成】C 61.28% H 4.29% F 8.08% N 5.95% O 20.41%

与该中间体有关的原料药合成路线共 2 条

合成路线1

该中间体在本合成路线中的序号:(I)

Title compound was synthesized by condensation of ethyl 6-fluoro-4-quinolone-3-carboxylate (I) with cyclohexylamine (II) in pyridine at 120 C under pressure.

1 Srivastava S; Srivastava, S.K.; Shukla, A.; Chauhan, P.M.; Puri, S.K.; Bhaduri, A.P.; Pandey, V.C.; Synthesis and methemoglobin toxicity of the amides of 6/7 mono or disubstituted quinolone. Bioorg Med Chem Lett 1999, 9, 1, 25.
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) 19903 ethyl 6-fluoro-4-oxo-1,4-dihydro-3-quinolinecarboxylate C12H10FNO3 详情 详情
(II) 17966 cyclohexanamine; cyclohexyl amine; cyclohexylamine 108-91-8 C6H13N 详情 详情

合成路线2

该中间体在本合成路线中的序号:(I)

Title compound was synthesized by condensation of ethyl 6-fluoro-4-quinolone-3-carboxylate (I) with N-methylpiperazine (II) in pyridine at 120 C under pressure.

1 Srivastava S; Srivastava, S.K.; Shukla, A.; Chauhan, P.M.; Puri, S.K.; Bhaduri, A.P.; Pandey, V.C.; Synthesis and methemoglobin toxicity of the amides of 6/7 mono or disubstituted quinolone. Bioorg Med Chem Lett 1999, 9, 1, 25.
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) 19903 ethyl 6-fluoro-4-oxo-1,4-dihydro-3-quinolinecarboxylate C12H10FNO3 详情 详情
(II) 10061 1-Methylpiperazine; 1-Methyl piperazine; N-Methylpiperazine 109-01-3 C5H12N2 详情 详情
Extended Information