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2-Methyl-4-nitrophenyl isocyanate → (4S)-2-(2-methyl4-nitrophenylimino)-3,4-diisobutyl-1,3-oxazolidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Methyl-4-nitrophenyl isocyanate | HCID 4296456 | — |
| 反応物 | HCID 22951243 | HCID 22951243 | — |
| 生成物 | (4S)-2-(2-methyl4-nitrophenylimino)-3,4-diisobutyl-1,3-oxazolidine | HCID 57001746 | — |
反応手順
(L)-Leucine methyl ester was reduced to (1S)-1-(hydroxymethyl)-3-methylbutylamine according to Method B1b, Step 2. The 2-hydroxyethylamine was reacted with isobutyraldehyde according to Method B4c, Step 1 to afford (4S)-2-isopropyl-4-isobutyl-1,3-oxazolidine. The oxazolidine was reduced according to Method B4c, Step 2 to give (1S)-1-(hydroxymethyl)-N-isobutyl-3-methylbutylamine. The substituted 2-hydroxyethylamine was reacted with SOCl2 according to Method B7b to give (1S)-1-(chloromethyl)-N-isobutyl-3-methylbutylamine. The chloroethylamine was reacted with 2-methyl-4-nitrophenyl isocyanate according to Method C4a to afford (4S)-2-(2-methyl-4-nitrophenylimino)-3,4-diisobutyl-1,3-oxazolidine.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06353006B1 |
| 出典データセット | uspto-grants-2002_03 |
| ORD ID | ord-ce7fa2cca60245afbdb2e6f302e9378a |
| 出典メモ | uspto-grants-2002_03 |