Hydrochloric Acid → HCID 67411425, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[C:11]1[O:12][C:13]2[C:18]([C:19](=[O:21])[CH:20]=1)=[C:17]([OH:22])[CH:16]=[C:15]([OH:23])[C:14]=2[C@@H:24]1[CH2:28][CH2:27][N:26]([CH3:29])[C@H:25]1[CH2:30][OH:31].Cl>CO>[ClH:1].[Cl:1][C:2]1[CH:7]=[C:6]([N+:8]([O-:10])=[O:9])[CH:5]=[CH:4][C:3]=1[C:11]1[O:12][C:13]2[C:18]([C:19](=[O:21])[CH:20]=1)=[C:17]([OH:22])[CH:16]=[C:15]([OH:23])[C:14]=2[C@@H:24]1[CH2:28][CH2:27][N:26]([CH3:29])[C@H:25]1[CH2:30][OH:31]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
(−)-trans-2-(2-Chloro-4-nitrophenyl)-5,7-dihydroxy-8-(2-hydroxymethyl-1-methyl pyrrolidin-3-yl)-chromen-4-one (0.2 g, 0.4 mmol) was suspended in methanol (10 mL) and treated with ethereal HCl and the organic solvent evaporated to get the title salt.
Workup
- customthe organic solvent evaporated
Sources & evidence
- ORD record
- ord-6b18e3e69e11428fb636ca60b7ca289a
- Source dataset
- uspto-grants-2013_10
- Patent number
- US08563596B2
Reaction notes
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