Hydrochloric Acid → Hydrochloric Acid
Reaction equation
[CH3:1][N:2]([CH3:15])[CH2:3][CH2:4][N:5]([CH3:14])[CH2:6][C:7]([O:9]C(C)(C)C)=[O:8].[ClH:16]>>[CH3:1][N:2]([CH3:15])[CH2:3][CH2:4][N:5]([CH3:14])[CH2:6][C:7]([OH:9])=[O:8].[ClH:16]Participants
4
Conditions
- Temperature
- 60 °C
Procedure
tert-Butyl 2-[[2-(dimethylamino)ethyl] (methyl)amino]acetate (1.25 g) prepared in Step A was added with 4 N hydrogen chloride (solution in 1,4-dioxane, 15 ml), and the mixture was stirred at 60° C. for 6 hours. The reaction mixture was cooled to room temperature, and the deposited solids were taken by filtration, washed with diethyl ether, and then dried under reduced pressure to obtain the title compound as hydrochloride (886 mg).
Workup
- temperatureThe reaction mixture was cooled to room temperature
- filtrationthe deposited solids were taken by filtration
- washwashed with diethyl ether
- customdried under reduced pressure
Sources & evidence
- ORD record
- ord-18437ca4ae6e4ccfa6ea34bce4d26bb6
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07964613B2
Reaction notes
Loading…