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HRID 276693作成日:2026年10月27日

Ethanolamine → (4S)-4-Isobutyl-2-isopropyloxazolidine

https://huagongshe.com/reaction/276693

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolamineHCID 700—
反応物IsobutyraldehydeHCID 6561—
反応物(+)-L-Leucine methyl esterHCID 65105—
反応物L-LeucinolHCID 111307—
生成物(4S)-4-Isobutyl-2-isopropyloxazolidineHCID 45096513—

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. 4-Amino-3-ethylbenzonitrile was converted to 4-cyano-2-ethylformanilide according to Method A3a, Step 1. The formanilide was reacted with SOCl2 and SO2Cl2 according to Method A3a, Step 2 to give 4-cyano-2-ethylphenyl isocyanide dichloride. The substituted 2-hydroxyethylamine was reacted with 4-cyano-2-ethylphenyl isocyanide dichloride according to Method C7b to afford (4S)-2-(4-cyano-2-ethylphenylimino)-3,4-diisobutyl-1,3-oxazolidine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06353006B1
出典データセットuspto-grants-2002_03
ORD IDord-c0e79a3d5de447a2ac3ee62c6d7421a8
出典メモuspto-grants-2002_03