1,4-Dioxane hydrochloride → N,N-dimethylazetidine-3-carboxamide hydrochloride

HRID 1799027Notes

Reaction equation

HRID 1799027 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

  1. concentrationThe reaction mixture was concentrated under reduced pressure, dioxane
  2. additionwas added to the obtained residue
  3. concentrationthe mixture was concentrated again under reduced pressure
  4. 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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