Hydrochloric Acid → HCID 20296962, compound
Reaction equation
[C:1]([C:5]1[C:14]2[CH2:13][CH2:12][CH2:11][CH2:10][C:9]=2[CH:8]=[C:7]([CH2:15][NH:16]C(=O)C)[C:6]=1[OH:20])(=[O:4])[CH2:2][CH3:3].[ClH:21]>CO>[ClH:21].[C:1]([C:5]1[C:14]2[CH2:13][CH2:12][CH2:11][CH2:10][C:9]=2[CH:8]=[C:7]([CH2:15][NH2:16])[C:6]=1[OH:20])(=[O:4])[CH2:2][CH3:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To 400 mg of the compound obtained in Example 4 (a) above were added 2 ml of methanol and 1 ml of concentrated hydrochloric acid followed by refluxing for 15 hours. The mixture was concentrated, and the residue was washed with diethyl ether and dissolved in methanol. Activated carbon was added to the solution which was then filtered. Diethyl ether was added to the filtrate and the precipitated crystals were filtered to obtain 160 mg of the title compound having the following physical properties.
Workup
- temperatureby refluxing for 15 hours
- concentrationThe mixture was concentrated
- washthe residue was washed with diethyl ether
- dissolutiondissolved in methanol
- additionActivated carbon was added to the solution which
- filtrationwas then filtered
- additionDiethyl ether was added to the filtrate
- filtrationthe precipitated crystals were filtered
Sources & evidence
- ORD record
- ord-e42e27bcb33c4aa8ac709b4e4cf7c552
- Source dataset
- uspto-grants-1981_01
- Patent number
- US04245099
Reaction notes
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