Hydrochloric Acid → HCID 22605931, compound
Reaction equation
[CH2:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][N:2]1[C:11]1[N:16]=[C:15]([C:17]([NH2:19])=O)[CH:14]=[CH:13][CH:12]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-].[ClH:26]>>[ClH:26].[CH2:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][N:2]1[C:11]1[N:16]=[C:15]([CH2:17][NH2:19])[CH:14]=[CH:13][CH:12]=1Participants
4
Procedure
Following the general method described in example 9, 6-(3,4-dihydro-1H-isoquinolin-2-yl)-pyridine-2-carboxylic acid amide (example 22a) was reacted with lithium aluminum hydride. After workup and chromatography the free base of the title compound was treated with hydrogen chloride and crystallized as the off white salt. Mp. 192-195° C. (iPr2O), MS: m/e=239 (M+).
Sources & evidence
- ORD record
- ord-ea826b4102004fc681a213fbab23ad78
- Source dataset
- uspto-grants-2004_12
- Patent number
- US06831087B2
Reaction notes
Loading…