3-Aminopyridine → HCID 77750225, 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].N[C:37]1[CH:38]=[N:39][CH:40]=CC=1>>[OH:35][CH:7]1[CH:8]([OH:34])[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)[CH2:10][CH:6]1[C:4]([NH:3][C:1]1[CH:40]=[N:39][CH:38]=[CH:37][CH:2]=1)=[O:5]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-aminopyridine.
Sources & evidence
- ORD record
- ord-5d186067d8964d80a6fd718bb2b497d4
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06369064B1
Reaction notes
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