2-N-cyclohexylpyridine-2,3-diamine → 3-Cyclooctyl-3H-imidazo[4,5-b]pyridine-2-amine
Reaction equation
[NH2:1][C:2]1[C:3]([NH:8][CH:9]2[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]2)=[N:4][CH:5]=[CH:6][CH:7]=1.[NH2:17][C:18]1C(NC2CCCCC2)=NC=CC=1>>[CH:9]1([N:8]2[C:3]3=[N:4][CH:5]=[CH:6][CH:7]=[C:2]3[N:1]=[C:18]2[NH2:17])[CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]1Participants
3
Procedure
The experimental protocol is identical with that used in Example 1, starting in Step a from 3-amino-2-cyclooctylaminopyridine of Preparation 3 instead of 3-amino-2-cyclohexylaminopyridine.
Sources & evidence
- ORD record
- ord-e6a7c11947ea4ca0a6586f1135d10672
- Source dataset
- uspto-grants-2006_08
- Patent number
- US07098220B2
Reaction notes
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