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HRID 276699作成日:2026年10月27日

Ethanolamine → 13-aza-6-oxadispiro[4.2.4.I]tridecane

https://huagongshe.com/reaction/276699

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolamineHCID 700—
反応物CycloleucineHCID 2901—
反応物CyclopentanoneHCID 8452—
反応物1-AminocyclopentanemethanolHCID 66307—
生成物13-aza-6-oxadispiro[4.2.4.I]tridecaneHCID 18316287—

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 hydroxyethylamine was reacted with cyclopentanone according to Method B4d, Step 1 to give 6-aza-12-oxadispiro[4.1.4.2]tridecane. The oxazolidine was reduced according to Method B4d, Step 2 to give 1-(cyclopentylamino)-1-(hydroxymethyl)cyclopentane. 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 2-methyl-4-nitrophenyl isocyanide dichloride according to Method C7a to afford 1-cyclopentyl-2-(2-methyl-4-nitrophenylimino)-3-oxa-1-azaspiro[4.4]nonane.

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-24f06a743e17471ba859c15d2e3ed75b
出典メモuspto-grants-2002_03