1,4-Dioxane hydrochloride → N,N-dimethylazetidine-3-carboxamide hydrochloride
Reaction equation
[CH3:1][N:2]([CH3:16])[C:3]([CH:5]1[CH2:8][N:7](C(OC(C)(C)C)=O)[CH2:6]1)=[O:4].[ClH:17].O1CCOCC1>>[ClH:17].[CH3:1][N:2]([CH3:16])[C:3]([CH:5]1[CH2:8][NH:7][CH2:6]1)=[O:4]Participants
3
Procedure
A mixture of t-butyl 3-dimethylcarbamoyl-azetidine-1-carboxylate (0.365 g) and 4N hydrogen chloride/dioxane solution (5 ml) was stirred at room temperature for 5 hr 15 min. The reaction mixture was concentrated under reduced pressure, dioxane was added to the obtained residue and the mixture was concentrated again under reduced pressure. The obtained residue was dried under reduced pressure at 60° C. to give the title compound (0.290 g). The obtained residue was directly used for the next reaction without further purification.
Workup
- concentrationThe reaction mixture was concentrated under reduced pressure, dioxane
- additionwas added to the obtained residue
- concentrationthe mixture was concentrated again under reduced pressure
- customThe obtained residue was dried under reduced pressure at 60° C.
Sources & evidence
- ORD record
- ord-3952b8cd197842188963e54652bc2976
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08343994B2
Reaction notes
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