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HRID 2370792作成日:2026年10月26日

1-Oxo-2,3-dihydro-1H-isoindole-5-carboxylic acid → (S)-1-oxo-N-((4-(trifluoromethyl)phenyl)(3-(trifluoromethyl)pyridin-2-yl)methyl)isoindoline-5-carboxamide

https://huagongshe.com/reaction/2370792

反応式

関与物質

役割名称HCID仕込み量
反応物1-Oxo-2,3-dihydro-1H-isoindole-5-carboxylic acidHCID 12850266—
反応物(S)-(4-(Trifluoromethyl)phenyl)(3-(trifluoromethyl)pyridin-2-yl)methanamine HydrochlorideHCID 86687962—
生成物(S)-1-oxo-N-((4-(trifluoromethyl)phenyl)(3-(trifluoromethyl)pyridin-2-yl)methyl)isoindoline-5-carboxamideHCID 86687968—

反応手順

1-Oxoisoindoline-5-carboxylic acid was then coupled with Intermediate 1 using the general methods described above for the amide coupling reaction (Table 2) to provide the title compound, (S)-1-oxo-N-((4-(trifluoromethyl)phenyl)(3-(trifluoromethyl)pyridin-2-yl)methyl)isoindoline-5-carboxamide, as a white solid. 1H NMR (400 MHz, CDCl3) δ ppm 8.92 (d, J=4.7 Hz, 1H), 8.36 (d, J=7.4 Hz, 1H), 8.09-7.99 (m, 2H), 7.97-7.88 (m, 2H), 7.65-7.53 (m, 5H), 7.51 (dd, J=4.9, 7.8 Hz, 1H), 6.90 (d, J=7.6 Hz, 1H), 4.54 (s, 2H). MS (ESI pos. ion) m/z: 480.2 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08710043B2
出典データセットuspto-grants-2014_04
ORD IDord-309d6dcc52424f45a90be9177b87ec7b
出典メモuspto-grants-2014_04