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HRID 445063作成日:2026年10月25日

2-Fluorophenethyl bromide → HCID 178492624、化合物

https://huagongshe.com/reaction/445063

反応式

関与物質

役割名称HCID仕込み量
反応物2-Fluorophenethyl bromideHCID 2756964—
反応物HCID 178492621HCID 178492621—
生成物HCID 178492624HCID 178492624—

反応手順

The title compounds were prepared from 8-(2,5-dimethoxy-phenylsulfanyl)-9H-purin-6-ylamine and 1-(2-bromo-ethyl)-2-fluoro-benzene by a procedure similar to examples 1 and 2. The isomers were separated by preparative HPLC. 8-(2,5-Dimethoxy-phenylsulfanyl)-9-[2-(2-fluoro-phenyl)-ethyl]-9H-purin-6-ylamine: Yield 37%, 1H NMR (DMSO-d6) δ 8.27 (s, 1H), 7.28-7.22 (m, 1H), 7.12-7.00 (m, 4H), 6.87 (dd, J=8.8, 3.2 Hz, 1H), 6.55 (d, J=3.2 Hz, 1H), 4.45 (t, J=6.8, Hz, 2H), 3.72 (s, 3H), 3.62 (s, 3H), 3.08 (t, J=6.8, 2H); LC-MS [M+H]+ 426.1. 8-(2,5-Dimethoxy-phenylsulfanyl)-3-[2-(2-fluoro-phenyl)-ethyl]-3H-purin-6-ylamine: Yield, 18%, 1H NMR (DMSO-d6) δ 8.37 (s, 1H), 8.19 (bs, 2H), 7.33-7.08 (m, 7H), 4.55 (t, J=7.2 Hz, 2H), 3.76 (s, 3H), 3.73 (s, 3H), 3.23 (t, J=7.2 Hz, 2H); LC-MS [M+H]+ 426.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08476285B2
出典データセットuspto-grants-2013_07
ORD IDord-8b3e29bf721b4f4a9dc2e2e2d0336229
出典メモuspto-grants-2013_07