HCID 88931008, compound → HCID 88931009, compound
Reaction equation
[Cl:1][C:2]1[C:7]2[C:8]([CH3:16])=[CH:9][N:10]([CH2:11][CH2:12][CH2:13][O:14][CH3:15])[C:6]=2[CH:5]=[C:4]([C:17](N(OC)C)=[O:18])[N:3]=1.[CH3:23][Mg]Br>>[Cl:1][C:2]1[C:7]2[C:8]([CH3:16])=[CH:9][N:10]([CH2:11][CH2:12][CH2:13][O:14][CH3:15])[C:6]=2[CH:5]=[C:4]([C:17](=[O:18])[CH3:23])[N:3]=1Participants
3
Procedure
4-Chloro-N-methoxy-1-(3-methoxypropyl)-N,3-dimethyl-1H-pyrrolo[3,2-c]pyridine-6-carboxamide and methylmagnesium bromide were treated in the similar manner to Reference Example 6(5) to give 1-[4-chloro-1-(3-methoxypropyl)-3-methyl-1H-pyrrolo[3,2-c]pyridin-6-yl]ethanone [REx(105-8)] as a colorless powder.
Sources & evidence
- ORD record
- ord-b87ecc2bfe874f5abcd3583e6cb21490
- Source dataset
- uspto-grants-2016_03
- Patent number
- US09278944B2
Reaction notes
Loading…