Methylamine → HCID 22386186, compound
Reaction equation
[Cl:1][C:2]1[C:3]([C:9]([N:11]([CH:20]([C:24]2[CH:29]=[CH:28][CH:27]=[C:26]([O:30][CH3:31])[CH:25]=2)[C:21]([NH2:23])=[O:22])[CH2:12][C:13]2[CH:18]=[CH:17][C:16]([CH3:19])=[CH:15][CH:14]=2)=[O:10])=[N:4][C:5]([NH2:8])=[N:6][CH:7]=1.[CH3:32]N>>[Cl:1][C:2]1[C:3]([C:9]([N:11]([CH:20]([C:24]2[CH:29]=[CH:28][CH:27]=[C:26]([O:30][CH3:31])[CH:25]=2)[C:21]([NH2:23])=[O:22])[CH2:12][C:13]2[CH:14]=[CH:15][C:16]([CH3:19])=[CH:17][CH:18]=2)=[O:10])=[N:4][C:5]([NH:8][CH3:32])=[N:6][CH:7]=1Participants
3
Procedure
This was prepared in the same manner as the product of example 249, using methylamine as the amine, to give the title compound as a foam, 0.24 g, (88%).
Sources & evidence
- ORD record
- ord-28b0b398442749049ff2dccbf0a2dbec
- Source dataset
- uspto-grants-2005_07
- Patent number
- US06914160B1
Reaction notes
Loading…