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2-(3-Chloro-6-oxo-1,6-dihydropyridazin-1-yl)acetic acid → 2-(6-Oxo-1,6-dihydropyridazin-1-yl)acetic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-(3-Chloro-6-oxo-1,6-dihydropyridazin-1-yl)acetic acid | HCID 5121297 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 2-(6-Oxo-1,6-dihydropyridazin-1-yl)acetic acid | HCID 1415536 | — |
反応手順
[3-Chloro-6-oxopyridazin-1(6H)-yl]acetic acid (1.00 g, 5.30 mmol) in methanol (40 mL) was added 100 mg of 10% Pd/C. After the reaction mixture was stirred at ambient temperature under a H2 balloon for 1 h, the Pd was filtered off through celite. The filtrate was concentrated in vacuo and purified by reverse phase HPLC (TMC Pro-Pac C18; 0-40% 0.1% trifluoroacetic acid in acetonitrile/0.1% trifluoroacetic acid in water gradient). Removal of the volatiles in vacuo afforded the title compound as a white crystalline. 1H NMR (D2O): δ 8.06 (dd, J=3.9, 1.4 Hz, 1H), 7.56 (dd, J=9.4, 3.9 Hz, 1H), 7.12 (dd, J=9.4, 1.5 Hz, 1H), 4.95 (s, 2H). LC/MS 155.2 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09186354B2 |
| 出典データセット | uspto-grants-2015_11 |
| ORD ID | ord-4553935253964522beebfc9925035ec3 |
| 出典メモ | uspto-grants-2015_11 |