HCID 57985899, compound → HCID 57985933, compound
Reaction equation
[CH3:1][NH:2][C:3](=[O:21])[CH2:4][CH:5]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)[C:6]1[C:14]2[C:9](=[N:10][CH:11]=[CH:12][CH:13]=2)[NH:8][CH:7]=1.[Cl:22]C1C=CN=C2NC=C(C(C3C=CC=CC=3)C3C(=O)OC(C)(C)OC3=O)C=12>>[Cl:22][C:13]1[CH:12]=[CH:11][N:10]=[C:9]2[NH:8][CH:7]=[C:6]([CH:5]([C:15]3[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=3)[CH2:4][C:3]([NH:2][CH3:1])=[O:21])[C:14]=12Participants
3
Procedure
3-(4-Chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-N-methyl-3-phenyl-propionamide was prepared (73% yield) following the procedure described for preparation of N-methyl-3-phenyl-3-(1H-pyrrolo[2,3-b]pyridin-3-yl)-propionamide in Example 1, using 5-[(4-chloro-1H-pyrrolo[2,3-b]pyridin-3-yl)-phenyl-methyl]-2,2-dimethyl-[1,3]dioxane-4,6-dione.
Sources & evidence
- ORD record
- ord-c85b69d0b7804d1796766220ae4f2d91
- Source dataset
- uspto-grants-2009_12
- Patent number
- US07638517B2
Reaction notes
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