HCID 66632182, compound → HCID 68296472, compound
Reaction equation
I[C:2]1[C:10]2[C:5](=[N:6][CH:7]=[CH:8][CH:9]=2)[N:4](C(OC(C)(C)C)=O)[C:3]=1C.[OH:19][CH2:20][CH2:21][N:22]1[CH:31]=[C:30](I)[C:29]2[C:24](=[CH:25][N:26]=[CH:27][CH:28]=2)[C:23]1=[O:33]>>[OH:19][CH2:20][CH2:21][N:22]1[CH:31]=[C:30]([C:2]2[C:10]3[C:5](=[N:6][CH:7]=[CH:8][CH:9]=3)[NH:4][CH:3]=2)[C:29]2[C:24](=[CH:25][N:26]=[CH:27][CH:28]=2)[C:23]1=[O:33]Participants
3
Procedure
Analogously to Example 5, tert-butyl 3-iodo-2-methylpyrrolo[2,3-b]pyridine-1-carboxylate is reacted with 2-(2-hydroxyethyl)-4-iodo-2H-2,7-naphthyridin-1-one, giving 2-(2-hydroxyethyl)-4-(1H-pyrrolo[2,3-b]pyridin-3-yl)-2H-2,7-naphthyridin-1-one as colourless solid; MS (ESI): 307 [M+H]+.
Sources & evidence
- ORD record
- ord-dc307eca41c243b781455e3ef48ff579
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08981101B2
Reaction notes
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