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HRID 37793作成日:2026年10月25日

4-Vinylpyridine → 7-[(E)-2-pyridin-4-ylvinyl]-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indole

https://huagongshe.com/reaction/37793

反応式

関与物質

役割名称HCID仕込み量
反応物4-VinylpyridineHCID 7502—
反応物Sulfuric acid magnesium salt (1:1)HCID 24083—
反応物7-bromo-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indoleHCID 67240163—
生成物7-[(E)-2-pyridin-4-ylvinyl]-3,4,5,6-tetrahydro-1H-2,5-ethanoazepino[4,3-b]indoleHCID 53251098—

反応手順

The product of Example 1B (100 mg, 0.34 mmol), 4-vinylpyridine (144 mg, 1.37 mmol; Aldrich) and MgSO4 (83 mg, 0.69 mmol) were combined and processed as described in Example 1D to provide the title compound: 1H NMR (400 MHz, methanol-d4) δ ppm 1.97-2.22 (m, 4 H), 3.03-3.12 (m, 2 H), 3.13-3.18 (m, 1 H), 3.21-3.29 (m, 2 H), 4.24 (s, 2 H), 7.04 (t, J=7.6 Hz, 1 H), 7.24 (d, J=16.5 Hz, 1 H), 7.31 (dd, J=7.8, 0.8 Hz, 1 H), 7.44 (d, J=7.6 Hz, 1 H), 7.59-7.69 (m, 2 H), 7.94 (d, J=16.5 Hz, 1 H), 8.46-8.50 (m, 2 H); MS (APCI) m/z 316 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524703B2
出典データセットuspto-grants-2013_09
ORD IDord-7ded72baff6e4dc2a6c0f5caf89b3cd0
出典メモuspto-grants-2013_09