참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethanolamine | HCID 700 | — |
| 반응물 | Isobutyraldehyde | HCID 6561 | — |
| 반응물 | (+)-L-Leucine methyl ester | HCID 65105 | — |
| 반응물 | L-Leucinol | HCID 111307 | — |
| 생성물 | (4S)-4-Isobutyl-2-isopropyloxazolidine | HCID 45096513 | — |
반응 단계
(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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06353006B1 |
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| 출처 데이터셋 | uspto-grants-2002_03 |
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| ORD ID | ord-c0e79a3d5de447a2ac3ee62c6d7421a8 |
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| 출처 메모 | uspto-grants-2002_03 |
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