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HRID 1742944作成日:2026年10月26日

5-Amino-1-(2,4-difluorophenyl)-6,7,8-trifluoro-1,4-dihydro-4-oxo-quinoline-3-carboxylic acid → 5-Amino-7-[cis-3-amino-4-(1,2,3-triazol-1-yl)-pyrrolidin-1-yl]-1-(2,4-difluorophenyl)-6,8-difluoro-1,4-dihydro-4-oxo-quinoline-3-carboxylic acid

https://huagongshe.com/reaction/1742944

反応式

関与物質

役割名称HCID仕込み量
反応物5-Amino-1-(2,4-difluorophenyl)-6,7,8-trifluoro-1,4-dihydro-4-oxo-quinoline-3-carboxylic acidHCID 14896552—
反応物rac-(3R,4S)-4-(1H-1,2,3-triazol-1-yl)pyrrolidin-3-amineHCID 70283180—
生成物5-Amino-7-[cis-3-amino-4-(1,2,3-triazol-1-yl)-pyrrolidin-1-yl]-1-(2,4-difluorophenyl)-6,8-difluoro-1,4-dihydro-4-oxo-quinoline-3-carboxylic acidHCID 7028258266%

反応手順

Prepared by following the same procedure as described for Example 17 by using 5-amino-1-(2,4-difluorophenyl) -6,7,8-trifluoro-1,4-dihydro-4-oxo-quinoline-3-carboxylic acid and cis-3-amino-4-(1,2,3-triazol-1-yl)-pyrrolidine. Yield: 66%, m.p. 279°-281° C. 1H NMR (TFA) δ: 4.48-4.82 (m, 4H), 5.02 (m, 1H), 6.26 (m, 1H), 7.17 (m, 2H), 7.62 (m, 1H), 8.6 (s, 1H), 8.82 (d, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05342846
出典データセットuspto-grants-1994_08
ORD IDord-393c0f69511f40e598d98e965662b115
出典メモuspto-grants-1994_08