Reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]([CH:15]=[CH:16][C:17]=1[OH:18])[C:5]([NH:7][CH:8]([CH2:12][CH2:13][CH3:14])[CH2:9][CH2:10][CH3:11])=[O:6].[CH2:19]([O:21][C:22](OCC)(OCC)OCC)[CH3:20]>>[CH2:9]([CH:8]([NH:7][C:5]([C:4]1[CH:15]=[CH:16][C:17]2[O:18][C:22]([O:21][CH2:19][CH3:20])=[N:1][C:2]=2[CH:3]=1)=[O:6])[CH2:12][CH2:13][CH3:14])[CH2:10][CH3:11]Participants
3
Procedure
Prepared in a similar manner to example 41 using 3-amino-4-hydroxy-N-(1-propylbutyl)benzamide (example 41a) and tetraethoxymethane: mp 128-129° C.; MS (M+H, 305.1).
Sources & evidence
- ORD record
- ord-fffb647961d44e0ebfdc4ba854e2dd49
- Source dataset
- uspto-grants-2014_11
- Patent number
- US08895050B2
Linked notes
Loading…