Hydrochloric Acid → HCID 19599930, compound
Reaction equation
[CH2:1]([N:3]([CH2:6][C:7]1[O:32][C:10]2[CH2:11][N:12]([C:15](=[O:31])[C:16]3[CH:21]=[CH:20][C:19]([C:22](=[O:30])[C:23]4[CH:28]=[CH:27][C:26]([Cl:29])=[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].Cl>CO>[ClH:29].[CH2:1]([N:3]([CH2:6][C:7]1[O:32][C:10]2[CH2:11][N:12]([C:15](=[O:31])[C:16]3[CH:21]=[CH:20][C:19]([C:22](=[O:30])[C:23]4[CH:24]=[CH:25][C:26]([Cl:29])=[CH:27][CH:28]=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-(4-chlorobenzoyl)benzoyl]-4,5,6,7-tetrahydrofuro[2,3-c]pyridin-2-ylmethyl]amine 1.047 g was dissolved in 2 ml of methanol; hydrogen chloride in methanol was added in excess, followed by stirring. This was concentrated to yield the desired product.
Workup
- concentrationThis was concentrated
Sources & evidence
- ORD record
- ord-f2e8e56667ca4d0c95351e258387fb9c
- Source dataset
- uspto-grants-1999_12
- Patent number
- US05998433
Reaction notes
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