2-Amino-2-methyl-1-propanol → HCID 22476538, compound
Reaction equation
OCCN[C:5](=[O:9])[C:6]([NH2:8])=[O:7].[NH2:10][C:11]([CH3:15])([CH3:14])[CH2:12][OH:13]>>[OH:13][CH2:12][C:11]([NH:10][C:5](=[O:9])[C:6]([NH2:8])=[O:7])([CH3:15])[CH3:14]Participants
3
Procedure
Prepared as in Intermediate 3, using 2-amino-2-methylpropanol. The product did not precipitate out, even on adding diethyl ether. The solution was passed through a SCX cartridge, to remove excess amine, then evaporated to give the title compound as a white powder (1.54 g, 96% ); NMR [(CD3)2SO] 1.25 (6H, s), 3.36 (2H, d), 5.07 (1H, t), 7.74 (1H, s), 7.78 (1H, br s), and 8.04 (1H, br s).
Workup
- customThe product did not precipitate out
- additioneven on adding diethyl ether
- customto remove excess amine
- customevaporated
Sources & evidence
- ORD record
- ord-d4f99591fd0b4d31bc7828a22203a044
- Source dataset
- uspto-grants-2007_01
- Patent number
- US07160907B2
Reaction notes
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