Hydrochloric Acid → HCID 68515008, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([NH:8][CH3:9])[CH:5]=[CH:4][C:3]=1[C:10]1[O:11][C:12]2[C:17]([C:18](=[O:20])[CH:19]=1)=[C:16]([OH:21])[CH:15]=[C:14]([OH:22])[C:13]=2[C@@H:23]1[CH2:27][CH2:26][N:25]([CH3:28])[C@H:24]1[CH2:29][OH:30].Cl>CO>[ClH:1].[Cl:1][C:2]1[CH:7]=[C:6]([NH:8][CH3:9])[CH:5]=[CH:4][C:3]=1[C:10]1[O:11][C:12]2[C:17]([C:18](=[O:20])[CH:19]=1)=[C:16]([OH:21])[CH:15]=[C:14]([OH:22])[C:13]=2[C@@H:23]1[CH2:27][CH2:26][N:25]([CH3:28])[C@H:24]1[CH2:29][OH:30]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The compound, (+)-trans-2-(2-Chloro-4-methylamino-phenyl)-5,7-dihydroxy-8-(2-hydroxymethyl-1-methyl-pyrrolidin-3-yl)-chromen-4-one (0.13 g, 0.3 mmol) was suspended in methanol (2 mL) and treated with ethereal HCl and the organic solvent evaporated to obtain the salt, (+)-trans-2-(2-chloro-4-methylaminophenyl)-5,7-dihydroxy-8-(2-hydroxymethyl-1-methyl-pyrrolidin-3-yl)-chromen-4-one hydrochloride.
Workup
- customthe organic solvent evaporated
Sources & evidence
- ORD record
- ord-2f68ed1944d24868b212d88989a1bb62
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08563596B2
Reaction notes
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