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HRID 984452作成日:2026年10月25日

2-Chlorobenzaldehyde → (2-Bromophenyl)[2-chloro-4-(E-((4-acetylhomopiperazin-1-yl)carbonyl) ethenyl)phenyl]sulfide

https://huagongshe.com/reaction/984452

反応式

関与物質

役割名称HCID仕込み量
反応物2-ChlorobenzaldehydeHCID 6996—
反応物6-Amino-1-hexanolHCID 19960—
反応物2,4-DichlorobenzenethiolHCID 70730—
反応物2-BromobenzenethiolHCID 80598—
反応物3-Chloro-4-fluorobenzaldehydeHCID 593866—
反応物N-AcetylhomopiperazineHCID 4186202—
生成物(2-Bromophenyl)[2-chloro-4-(E-((4-acetylhomopiperazin-1-yl)carbonyl) ethenyl)phenyl]sulfideHCID 9805756—

反応手順

The title compound was prepared by the procedures described in Example 1 substituting 2,4-dichlorothiophenol with 2-bromothiophenol, 2-chlorobenzaldehyde with 3-chloro-4-fluoro-benzaldehyde, and 6-amino-1-hexanol with 4-acetylhomopiperazine. 1H NMR (DMSO-d6, 300 MHz) δ 8.10 (m, 1H), 7.81 (d, J=7.7 Hz, 1H), 7.64 (m, 1H), 7.24-7.51 (m, 5H), 7.05 (m, 1H), 3.39-3.77 (m, 8H), 1.97 (m, 3H), 1.68 (m, 2H). HRMS calculated for C22H22N2O2S1Br1Cl1: 493.0352. Observed: 493.0352.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06867203B2
出典データセットuspto-grants-2005_03
ORD IDord-6cfc7eeaddbd4060b1b42150ac8e0929
出典メモuspto-grants-2005_03