Hydrochloric Acid → N,N-dimethyl-[6-(anthraquinone-2-carbonyl)-4,5,6,7-tetrahydrofuro[2,3-c]pyridin-2-ylmethyl]amine hydrochloride
Reaction equation
[CH3:1][N:2]([CH2:4][C:5]1[O:31][C:8]2[CH2:9][N:10]([C:13]([C:15]3[CH:28]=[CH:27][C:26]4[C:25](=[O:29])[C:24]5[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=5)[C:18](=[O:30])[C:17]=4[CH:16]=3)=[O:14])[CH2:11][CH2:12][C:7]=2[CH:6]=1)[CH3:3].[ClH:32]>CO.C(OCC)(=O)C>[ClH:32].[CH3:3][N:2]([CH2:4][C:5]1[O:31][C:8]2[CH2:9][N:10]([C:13]([C:15]3[CH:28]=[CH:27][C:26]4[C:25](=[O:29])[C:24]5[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=5)[C:18](=[O:30])[C:17]=4[CH:16]=3)=[O:14])[CH2:11][CH2:12][C:7]=2[CH:6]=1)[CH3:1]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
N,N-Dimethyl-[6-(anthraquinone-2-carbonyl)-4,5,6,7-tetrahydrofuro[2,3-c]pyridin-2-ylmethyl]amine 0.227 g was dissolved in 2 ml of methanol; hydrogen chloride in ethyl acetate was added in excess, followed by stirring. After this mixture was concentrated, the resulting solid was recrystallized from diethyl ether-ethanol to yield the desired product.
Workup
- concentrationAfter this mixture was concentrated
- customthe resulting solid was recrystallized from diethyl ether-ethanol
Sources & evidence
- ORD record
- ord-b46d223629d840bf9c83f1f44c2d76e3
- Source dataset
- uspto-grants-1999_12
- Patent number
- US05998433
Reaction notes
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