Propanolamine ethyl ether → HCID 77750168, compound
Reaction equation
[CH2:1]([NH:3][C:4]([CH:6]1[CH2:10][CH:9]([N:11]2[C:15]3[N:16]=[C:17]([S:30][CH2:31][CH2:32][CH3:33])[N:18]=[C:19]([NH:20][CH:21]4[CH2:23][CH:22]4[C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=4)[C:14]=3[N:13]=[N:12]2)[CH:8]([OH:34])[CH:7]1[OH:35])=[O:5])[CH3:2].[CH2:36]([O:38][CH2:39]CCN)[CH3:37]>>[CH2:36]([O:38][CH2:39][CH2:2][CH2:1][NH:3][C:4]([CH:6]1[CH2:10][CH:9]([N:11]2[C:15]3[N:16]=[C:17]([S:30][CH2:31][CH2:32][CH3:33])[N:18]=[C:19]([NH:20][CH:21]4[CH2:23][CH:22]4[C:24]4[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=4)[C:14]=3[N:13]=[N:12]2)[CH:8]([OH:34])[CH:7]1[OH:35])=[O:5])[CH3:37]Participants
3
Procedure
The subtitle compound was prepared according to the method of example 39, step a) using the product of example 1, step c) and 3-ethoxypropylamine.
Sources & evidence
- ORD record
- ord-af5b4a92b4664d5e88e9c87beef878bf
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06369064B1
Reaction notes
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