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HRID 2103491作成日:2026年10月27日

Phenylacetyl chloride → N-[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4-yl]-2-phenylacetamide

https://huagongshe.com/reaction/2103491

反応式

関与物質

役割名称HCID仕込み量
反応物Phenylacetyl chlorideHCID 7679—
反応物PomalidomideHCID 134780—
溶媒TetrahydrofuranHCID 8028—
生成物N-[2-(2,6-dioxo(3-piperidyl))-1,3-dioxoisoindolin-4-yl]-2-phenylacetamideHCID 1027174492%

反応手順

To a stirred suspension of 4-amino-2-(2,6-dioxo(3-piperidyl))isoindoline-1,3-dione (0.55 g, 2.0 mmol) in THF (30 ml) was added 2-phenylacetyl chloride (0.62 g, 4.0 mmol). The mixture was heated to reflux for 18 hours. The solvent was evaporated in vacuo and the resulting solid was slurried in diethyl ether (20 ml) and filtered to give 0.72 g (92%) of product as an off-white solid: mp 217-218° C.; 1H NMR (DMSO-d6) δ 11.15 (s, 1H), 9.79 (s, 1H), 8.49 (d, J=8.4 Hz, 1H), 7.82 (t, J=7.9 Hz, 1H), 7.60 (t, J=7.3 Hz, 1H), 7.41-7.27 (m, 5H), 5.13 (dd, J=5.1 and 12.7 Hz, 1H), 3.85 (s, 2H), 2.98-2.83 (m, 1H), 2.64-2.44 (m, 2H), 2.08-2.04 (m, 1H); 13C NMR (DMSO-d6) δ 172.71, 170.07, 169.74, 167.60, 166.61, 136.38, 136.10, 134.70, 131.41, 129.41, 128.58, 126.97, 125.96, 118.39, 116.90, 48.89, 43.47, 30.90, 21.91; Anal. Calcd For C21H17N3O5: C, 64.45; H, 4.38; —N, 10.74. Found: C, 64.23; H, 4.34; N, 10.53.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07576104B2
出典データセットuspto-grants-2009_08
ORD IDord-1de4d667e3fb4c92a3f10a7beb6b404b
出典メモuspto-grants-2009_08