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phosphenous acid → 3(s)-(4-Chloro-phenyl)-2(s)-ethyl-n-hydroxy-4-morpholin-4-yl-4-oxo-butyramide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | phosphenous acid | HCID 22497 | — |
| 反応物 | O-(Trimethylsilyl)hydroxylamine | HCID 2734666 | — |
| 反応物 | 3(S)-(4-Chloro-phenyl)-2(S)-ethyl-4-morpholin-4-yl-4-oxo-butyric acid | HCID 11313374 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 3(s)-(4-Chloro-phenyl)-2(s)-ethyl-n-hydroxy-4-morpholin-4-yl-4-oxo-butyramide | HCID 9927931 | — |
反応手順
The crude acid 1b (310 mg, 0.95 mmol) was dissolved in 5 ml of dichloromethane. HOPO (111 mg, 1 mmol) and MEI (0.159 ml, 1.14 mmol) were added successively. The mixture was stirred for 30 minutes, then TMSONH2 (0.233 ml, 1.9 mmol) was added. After one hour another portion of TMSONH2 (0.233 ml, 1.9 mmol) was added and stirring continued over night. The reaction mixture was filtered (solid contained mostly HOPO) diluted with 20 ml of dichloromethane and extracted twice with 2N-HCl and brine, dried over anhydrous sodium sulfate and evaporated. The crude solid (237 mg, 73%) was purified by preparative HPLC (methanol/water=1/1). Yield: 100 mg (31%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07589091B2 |
| 出典データセット | uspto-grants-2009_09 |
| ORD ID | ord-d2f47feed4234b039e031033850dfaa3 |
| 出典メモ | uspto-grants-2009_09 |