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Potassium Carbonate → [4-Oxo-4-phenyl-3-(2-pyridinyl)butylidene]bisphosphonic acid tetraethyl ester hemihydrate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Tetraethyl vinylidene phosphonate | HCID 11022954 | — |
| 反応物 | N-(6-methoxybenzothiazol-2-yl)-3-oxo-3-phenylpropanamide | HCID 19975336 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | [4-Oxo-4-phenyl-3-(2-pyridinyl)butylidene]bisphosphonic acid tetraethyl ester hemihydrate | HCID 131718992 | — |
反応手順
Ethenylidenebisphosphonic acid tetraethyl ester (I, 3.00 g), 1-phenyl-2-(2-pyridinyl)ethanone (II, 2.17 g) and potassium carbonate (2.07 g) are stirred in methanol (20 ml) overnight. The reaction is concentrated under reduced pressure, taken up in ethyl acetate, washed with sodium chloride, dried with magnesium sulfate, and concentrated under reduced pressure. The product is chromatographed eluting with ethyl acetate. The appropriate fractions are pooled and concentrated to give the title compound, MS (m/e) 497, 452, 392, 302 and 288; IR (neat) 2983, 1683, 1597, 1580, 1470, 1448 and 1253 cm-1 ; NMR (CDCl3) 8.52, 8.02, 7.60, 7.49, 7.37, 7.11, 5.46, 4.12, 2.75, 2.55, 1.36, 1.25 and 1.16 δ.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05412141 |
| 出典データセット | uspto-grants-1995_05 |
| ORD ID | ord-11b6ca9ebeb54b8eaeeb3093531cc74c |
| 出典メモ | uspto-grants-1995_05 |