Ethanolamine → HCID 18316174, compound
Reaction equation
[OH:1][CH2:2][CH2:3][NH2:4].[C:5]1(=O)[CH2:9][CH2:8][CH2:7][CH2:6]1>>[O:1]1[C:5]2([CH2:9][CH2:8][CH2:7][CH2:6]2)[NH:4][CH2:3][CH2:2]1Participants
3
Procedure
2-Hydroxyethylamine and cyclopentanone were reacted according to Method B4b, Step 1 to afford 4-aza-1-oxaspiro[4.4]nonane. The oxazolidine was reduced according to method B4b, Step 2 to afford N-cyclopentyl-N-(2-hydroxyethyl)amine. The alcohol was reacted with SOCl2 according to Method B7c to afford N-cyclopentyl-N-(2-chloroethyl)amine. The amine was reacted with 2-methoxy-4-nitrophenyl isothiocyanate according to Method C1d to afford 2-(2-methoxy-4-nitrophenylimino)-3-(cyclopentyl)-1,3-thiazolidine.
Sources & evidence
- ORD record
- ord-0cc5197d24474c549a75c6e1ec5c71d6
- Source dataset
- uspto-grants-2002_03
- Patent number
- US06353006B1
Reaction notes
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