Isobutyraldehyde → (S)-1-cyclopropyl-3-(4-(6-isobutyl-4-(3-methylmorpholino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-yl)phenyl)urea
Reaction equation
[CH:1]1([NH:4][C:5]([NH:7][C:8]2[CH:13]=[CH:12][C:11]([C:14]3[N:15]=[C:16]([N:23]4[CH2:28][CH2:27][O:26][CH2:25][C@@H:24]4[CH3:29])[C:17]4[CH2:22][NH:21][CH2:20][C:18]=4[N:19]=3)=[CH:10][CH:9]=2)=[O:6])[CH2:3][CH2:2]1.[CH:30](=O)[CH:31]([CH3:33])[CH3:32]>>[CH:1]1([NH:4][C:5]([NH:7][C:8]2[CH:9]=[CH:10][C:11]([C:14]3[N:15]=[C:16]([N:23]4[CH2:28][CH2:27][O:26][CH2:25][C@@H:24]4[CH3:29])[C:17]4[CH2:22][N:21]([CH2:30][CH:31]([CH3:33])[CH3:32])[CH2:20][C:18]=4[N:19]=3)=[CH:12][CH:13]=2)=[O:6])[CH2:2][CH2:3]1Participants
3
Procedure
Method as described for example 26 using (S)-1-cyclopropyl-3-(4-(4-(3-methylmorpholino)-6,7-dihydro-5H-pyrrolo[3,4-d]pyrimidin-2-yl)phenyl)urea (example 3) and iso-butyraldehyde as starting materials. Purified by prep HPLC (low pH).
Workup
- customPurified by prep HPLC (low pH)
Sources & evidence
- ORD record
- ord-94b09b8429a14256adb38375d7703152
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08785457B2
Reaction notes
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