Hydroxylamine → HCID 22575065, compound
Reaction equation
[NH:1]([CH2:5][C:6]([O-:8])=O)[C:2]([NH2:4])=[O:3].[NH2:9][OH:10]>O1CCOCC1>[OH:10][NH:9][C:6](=[O:8])[CH2:5][NH:1][C:2]([NH2:4])=[O:3]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A stock solution of triphosgene was prepared from solid triphosgene (1.48 g, 5 mmol) and DCM (20 mL). The solution was cooled to −78° C. and triethylamine (2 mL, 15 mmol) was slowly added. To ArgoGel-Wang or ArgoGel-OH resin bound 2-aminoacetate 4 (0.5 g) was added the triphosgene solution (3.5 mL) and the resin was shaken at rt for 1 h. The resin was drained, washed with DCM (3×) and then suspended in a solution of secondary amine 7 (e.g., pyrrolidine, 2 mmol) and TEA (3 mmol) in DCM (2 mL). After 16 h, the resin was washed with DCM and MeOH (3× each) to yield ArgoGel-Wang or ArgoGel-OH resin bound 2-ureidoacetate 6 which was then treated with a solution of aqueous 50% hydroxylamine (2 mL) and dioxane (1 mL) for 2 days. The resin was filtered, washed with acetonitrile and the filtrates combined and purified by preparative reverse-phase (C18) HPLC to yield product N-hydroxy-2-ureidoacetamide (I).
Workup
- filtrationThe resin was filtered
- washwashed with acetonitrile
- custompurified by preparative reverse-phase (C18) HPLC
Sources & evidence
- ORD record
- ord-82642b1d5fba4aeea530286b84aa0e7f
- Source dataset
- uspto-grants-2005_02
- Patent number
- US06852752B2
Reaction notes
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