3-ethoxypyridin-2-amine → HCID 66872573, compound
Reaction equation
[N:1]1([S:6]([C:9]2[CH:10]=[C:11]([CH:15]=[CH:16][CH:17]=2)[C:12]([OH:14])=O)(=[O:8])=[O:7])[CH2:5][CH2:4][CH2:3][CH2:2]1.[CH2:18]([O:20][C:21]1[C:22]([NH2:27])=[N:23][CH:24]=[CH:25][CH:26]=1)[CH3:19]>>[CH2:18]([O:20][C:21]1[C:22]([NH:27][C:12](=[O:14])[C:11]2[CH:15]=[CH:16][CH:17]=[C:9]([S:6]([N:1]3[CH2:2][CH2:3][CH2:4][CH2:5]3)(=[O:7])=[O:8])[CH:10]=2)=[N:23][CH:24]=[CH:25][CH:26]=1)[CH3:19]Participants
3
Procedure
The entitled compound was produced according to the method of Example 92 but using 3-(pyrrolidin-1-ylsulfonyl)benzoic acid and 3-ethoxypyridine-2-amine as the starting materials.
Workup
- customThe entitled compound was produced
Sources & evidence
- ORD record
- ord-240f2f776d1a4e619e4875ee9d7f72ce
- Source dataset
- uspto-grants-2013_04
- Patent number
- US08420823B2
Reaction notes
Loading…