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Benzoyl chloride → tetraethyl N-benzoyl-5-aminopentane-1,1-bisphosphonate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzoyl chloride | HCID 7412 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Tetraethyl 5-aminopentane-1,1-bisphosphonate | HCID 12102991 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | tetraethyl N-benzoyl-5-aminopentane-1,1-bisphosphonate | HCID 19689031 | 30.7% |
反応手順
A solution of benzoyl chloride (0.73 g, 5.0 mmol) in dichloromethane was added slowly to a solution of tetraethyl 5-aminopentane-1,1-bisphosphonate (1.50 g, 4.5 mmol) from Example 11, part A, and triethylamine (0.76 mL, 5.5 mmol) in dichloromethane at 0° C. After warming to room temperature for 30 minutes, the reaction was quenched by addition of 1N HCl (30 mL). The product was extracted into dichloromethane (2×20 mL) and the combined organic layers were washed with saturated NaHCO3 (2×15 mL), dried (Na2SO4), and concentrated in vacuo. Flash chromatography on silica gel eluting with 15% i-propanol in ethylacetate in EtOAc gave the title compound (0.64 g) as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05728650 |
| 出典データセット | uspto-grants-1998_03 |
| ORD ID | ord-18119a89941c4368a7ad288ebe54d59f |
| 出典メモ | uspto-grants-1998_03 |