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HRID 71319作成日:2026年10月25日

2,4-Dichloro-5-fluoropyrimidine → 2-chloro-5-fluoro-N4-(1,2,3,4-tetrahydro-1-oxonaphthalen-7-yl)-4-pyrimidineamine

https://huagongshe.com/reaction/71319

反応式

関与物質

役割名称HCID仕込み量
反応物2,4-Dichloro-5-fluoropyrimidineHCID 250705—
反応物7-Amino-1,2,3,4-tetrahydronaphthalen-1-oneHCID 327177—
生成物2-chloro-5-fluoro-N4-(1,2,3,4-tetrahydro-1-oxonaphthalen-7-yl)-4-pyrimidineamineHCID 22060787—

反応手順

In a like manner to the preparation of 2-chloro-N4-(3,4-ethylenedioxyphenyl)-5-fluoro-4-pyrimidineamine, 2,4-dichloro-5-fluoropyrimidine and 7-amino-1-tetralone were reacted to provide 2-chloro-5-fluoro-N4-(1,2,3,4-tetrahydro-1-oxonaphthalen-7-yl)-4-pyrimidineamine. 1H NMR (DMSO-d6): δ 10.08 (s, 1H), 8.31 (d, 1H, J=3.3 Hz), 8.15 (d, 1H, J=2.4 Hz), 7.82 (dd, 1H, J=2.4 and 8.1 Hz), 7.36 (d, 1H, J=8.1 Hz), 2.91 (t, 2H, J=6.0 Hz), 2.59 (t, 2H, J=6.0 Hz), 2.07-1.98 (m, 2H); LCMS: purity: 93%; MS (m/e): 294 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822685B2
出典データセットuspto-grants-2014_09
ORD IDord-e0274e8dbd444e709739609123c83835
出典メモuspto-grants-2014_09