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(4R,5S)-(+)-4-Methyl-5-phenyl-2-oxazolidinone → {3-[4-Bromo-2-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-ylmethyl)-phenoxy]-5-chloro-phenyl}-acetic acid ethyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (4R,5S)-(+)-4-Methyl-5-phenyl-2-oxazolidinone | HCID 2733812 | — |
| 反応物 | [3-(4-Bromo-2-bromomethyl-phenoxy)-5-chloro-phenyl]-acetic acid ethyl ester | HCID 58237642 | — |
| 生成物 | {3-[4-Bromo-2-((4R,5S)-4-methyl-2-oxo-5-phenyl-oxazolidin-3-ylmethyl)-phenoxy]-5-chloro-phenyl}-acetic acid ethyl ester | HCID 58237545 | — |
反応手順
Prepared according to the procedure described in Example 24, Step 7, using the following starting materials: [3-(4-bromo-2-bromomethyl-phenoxy)-5-chloro-phenyl]-acetic acid ethyl ester and (4R,5S)-4-methyl-5-phenyl-2-oxazolidinone.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08242145B2 |
| 出典データセット | uspto-grants-2012_08 |
| ORD ID | ord-bb3d09b858e24170b49d78ce46afcc1d |
| 出典メモ | uspto-grants-2012_08 |