2-Propanol, 1-amino-2-methyl- → HCID 70098086, compound
Reaction equation
[NH2:1][CH2:2][C:3]([CH3:6])([OH:5])[CH3:4].[CH:7]1([C:10]2[N:15]=[C:14]([C:16]([NH:18][C:19]3[CH:27]=[N:26][CH:25]=[CH:24][C:20]=3[C:21](O)=[O:22])=[O:17])[C:13]([NH:28][C:29]3[CH:30]=[N:31][CH:32]=[N:33][CH:34]=3)=[CH:12][CH:11]=2)[CH2:9][CH2:8]1>>[OH:5][C:3]([CH3:6])([CH3:4])[CH2:2][NH:1][C:21]([C:20]1[CH:24]=[CH:25][N:26]=[CH:27][C:19]=1[NH:18][C:16]([C:14]1[C:13]([NH:28][C:29]2[CH:30]=[N:31][CH:32]=[N:33][CH:34]=2)=[CH:12][CH:11]=[C:10]([CH:7]2[CH2:9][CH2:8]2)[N:15]=1)=[O:17])=[O:22]Participants
3
Procedure
According to the general method described in step 3 of example 53, reaction of 1-amino-2-methyl-propan-2-ol with 3-{[6-cyclopropyl-3-(pyrimidin-5-ylamino)-pyridine-2-carbonyl]-amino}-isonicotinic acid provided the title compound (28%) as amorphous yellow solid.
Sources & evidence
- ORD record
- ord-4ff4d8b14e7f475893a6f7b20187833b
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08703768B2
Reaction notes
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