Hydrochloric Acid → HCID 19600006, compound
Reaction equation
[CH2:1]([N:3]([CH2:6][C:7]1[O:31][C:10]2[CH2:11][N:12]([C:15](=[O:30])[C:16]3[CH:21]=[CH:20][C:19]([C:22](=[O:29])[C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=4)=[CH:18][CH:17]=3)[CH2:13][CH2:14][C:9]=2[CH:8]=1)[CH2:4][CH3:5])[CH3:2].[ClH:32]>CO>[ClH:32].[CH2:1]([N:3]([CH2:6][C:7]1[O:31][C:10]2[CH2:11][N:12]([C:15](=[O:30])[C:16]3[CH:21]=[CH:20][C:19]([C:22](=[O:29])[C:23]4[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=4)=[CH:18][CH:17]=3)[CH2:13][CH2:14][C:9]=2[CH:8]=1)[CH2:4][CH3:5])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
N,N-Diethyl-[6-(4-benzoylbenzoyl)-4,5,6,7-tetrahydrofuro[2,3-c]pyridin-2-ylmethyl]amine 0.423 g was dissolved in 2 ml of methanol; hydrogen chloride in methanol was added in excess, followed by stirring. This mixture was concentrated to yield the desired product.
Workup
- concentrationThis mixture was concentrated
Sources & evidence
- ORD record
- ord-e6084c8bf0064144a3eeac7801f96614
- Source dataset
- uspto-grants-1999_12
- Patent number
- US05998433
Reaction notes
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