関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tributylphosphine | HCID 13831 | — |
| 反応物 | 2,2,2-Trichloroethyl isoxazol-3-ylcarbamate | HCID 1211419 | — |
| 反応物 | diazenedicarboxylic acid bis(N,N-piperidide) | HCID 5702657 | — |
| 反応物 | (5R)-3-(3-fluoro-4-morpholin-4-ylphenyl)-5-(hydroxymethyl)-1,3-oxazolidin-2-one | HCID 10541953 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (5S)-3-(3-fluoro-4-morpholino-phenyl)-5-[(isoxazol-3-ylamino)methyl]oxazolidin-2-one | HCID 497405 | 331.2% |
反応手順
To a stirred solution of 3-(2,2,2-trichloroethyloxycarbonylamino)isoxazole (260 mg, 1.0 mmol), 5(R)-hydroxymethyl-3-(3-fluoro-4-morpholinophenyl)oxazolidin-2-one (see WO 95/07271; 293 mg, 1 mmol) and tributylphosphine (303 mg, 1.5 mmol) in dry tetrahydrofuran (10 ml) at 0° C. under a nitrogen atmosphere, was added 1,1-(azodicarbonyl)dipiperidine (378.5 mg, 1.5 mmol) in dry tetrahydrofuran (3 ml). The reaction allowed to warm to room temperature and was stirred for 4 days by which time a white suspension had formed. The reaction mixture was filtered and the residue washed with tetrahydrofuran. The filtrate was concentrated by rotary evaporation to give a yellow oil (1.2 g) which was purified by MPLC (30% ethyl acetate/hexane, ICN Alumina N 32–63) and further MPLC (100% CH2Cl2, ICN Alumina N 32–63). Concentration of the fractions by rotary evaporation gave the title compound as a crisp white foam (296 mg, 55%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07087629B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-302209980d6547c5afc3a3106403db72 |
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| 出典メモ | uspto-grants-2006_08 |
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