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HRID 413146作成日:2026年10月25日

(4-Amino-3'-chloro-biphenyl-3-yl)-propynyl-methanone → (4-Amino-3'-chloro-biphenyl-3-yl)-dipropynyl-methanol

https://huagongshe.com/reaction/413146

反応式

関与物質

役割名称HCID仕込み量
反応物(4-Amino-3'-chloro-biphenyl-3-yl)-propynyl-methanoneHCID 23509596—
反応物HCID 178419101HCID 178419101—
生成物(4-Amino-3'-chloro-biphenyl-3-yl)-dipropynyl-methanolHCID 22736629—

反応手順

Following the procedure of Example 41, (4-amino-3′-chloro-biphenyl-3-yl)-propynyl-methanone (mp 112-114° C.; MS ((+) ESI) m/z 270/272 (M+H)+) was treated with propynylmagnesium bromide to give (4-amino-3′-chloro-biphenyl-3-yl)-dipropynyl-methanol which was reacted with 1,1′-carbonyldiimidazole to afford the title compound. Yellow solid: mp 151° C. (decomposed); 1H-NMR (DMSO-d6) δ10.8 (s, 1H), 7.71 (dd, 1H, J=8.52,1.94 Hz), 7.69 (m, 2H), 7.61 (d, 1H, J=7.64 Hz), 7.50 (t, 1H, J=7.85 Hz), 7.43 (d, 1H, J=7.99 Hz), 7.06 (d, 1H, J=8.23 Hz), 2.0 (s, 6H); MS (APCI) m/z 336 ([M+H]+, 20%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06566358B2
出典データセットuspto-grants-2003_05
ORD IDord-8d3b24a94f9444269abd7ca3ac1276c0
出典メモuspto-grants-2003_05