関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethanolamine | HCID 700 | — |
| 反応物 | Cycloleucine | HCID 2901 | — |
| 反応物 | Cyclobutanone | HCID 14496 | — |
| 反応物 | 1-Aminocyclopentanemethanol | HCID 66307 | — |
| 生成物 | 5-Aza-12-oxadispiro[3.1.4.2]dodecane | HCID 18315997 | — |
反応手順
1-Aminocyclopentanecarboxylic acid was converted to the methyl ester according to Method B1c, Step 1. The ester reduced to 1-hydroxymethylcyclopentanamine according to Method B1c, Step 2. The 2-hydroxyethylamine was reacted with cyclobutanone according to Method B4a, Step 1 to give 5-aza-12-oxadispiro[3.1.4.2]dodecane. The oxazolidine was reduced according to Method B4a, Step 2 to give 1-(cyclobutylamino)-1-(hydroxymethyl)cyclopentane. The substituted 2-hydroxyethylamine was reacted with SOCl2 according to Method B7b to 1-(cyclobutylamino)-1-(chloromethyl)cyclopentane. The 2-chloroethylamine was reacted with 2-methyl-4-nitrophenyl isocyanate according to Method C4a to afford 1-cyclobutyl-2-(2-methyl-4-nitrophenylimino)-3-oxa-1-azaspiro[4.4]nonane.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06353006B1 |
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| 出典データセット | uspto-grants-2002_03 |
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| ORD ID | ord-b05a1cb0c8cf4b88846bcea17b61aa10 |
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| 出典メモ | uspto-grants-2002_03 |
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