1H-Pyrrolo[3,2-b]pyridine-2-carboxylic acid, methyl ester → {1H-pyrrolo[3,2-b]pyridin-2-yl}methanamine
Reaction equation
[NH:1]1[C:9]2[C:4](=[N:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[C:10](OC)=O.[NH:14]1C2=NC=CC=C2C=C1CN>>[NH:1]1[C:9]2[C:4](=[N:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[CH2:10][NH2:14]Participants
3
Procedure
Intermediate I was prepared from methyl 1H-pyrrolo[3,2-b]pyridine-2-carboxylate (1-1) following similar procedures for synthesizing intermediate H, as described above. MS (m/z): 148 (M+1)+.
Sources & evidence
- ORD record
- ord-b5b2e4ce1b0d47acbf24a609ac2f8725
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08507487B2
Reaction notes
Loading…