1-Cyclobutylmethanamine hydrochloride → 7-chloro-N-(cyclobutylmethyl)-1H-pyrrolo[2,3-c]pyridine-4-carboxamide
Reaction equation
[Cl:1][C:2]1[C:7]2[NH:8][CH:9]=[CH:10][C:6]=2[C:5]([C:11]([OH:13])=O)=[CH:4][N:3]=1.Cl.[CH:15]1([CH2:19][NH2:20])[CH2:18][CH2:17][CH2:16]1>>[CH:15]1([CH2:19][NH:20][C:11]([C:5]2[C:6]3[CH:10]=[CH:9][NH:8][C:7]=3[C:2]([Cl:1])=[N:3][CH:4]=2)=[O:13])[CH2:18][CH2:17][CH2:16]1Participants
3
Procedure
Prepared in a similar manner to Example 19 (e) from 7-chloro-1H-pyrrolo[2,3-c]pyridine-4-carboxylic acid using cyclobutylmethylamine hydrochloride (46 mg) instead of tetrahydro-pyran-4-ylmethylamine to give the title compound (39 mg).
Sources & evidence
- ORD record
- ord-8ea13bc326cc4625be04bed8be36d4b7
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07589206B2
Reaction notes
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