Hydrochloric Acid → HCID 135841608, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:25]=[CH:26][C:27]=1[O:28]COC)/[CH:6]=[CH:7]/[C:8]1[NH:16][C:15]2[C:14](=[O:17])[N:13]([CH2:18][CH2:19][CH3:20])[C:12](=[O:21])[N:11]([CH2:22][CH2:23][CH3:24])[C:10]=2[N:9]=1.Cl.[OH-].[Na+].O>O1CCCC1>[OH:28][C:27]1[CH:26]=[CH:25][C:5](/[CH:6]=[CH:7]/[C:8]2[NH:16][C:15]3[C:14](=[O:17])[N:13]([CH2:18][CH2:19][CH3:20])[C:12](=[O:21])[N:11]([CH2:22][CH2:23][CH3:24])[C:10]=3[N:9]=2)=[CH:4][C:3]=1[O:2][CH3:1]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Compound 194 (1.00 g, 2.33 mmol) obtained in Reference Example 133 was dissolved in 10 ml of tetrahydrofuran. To the solution was added 6 ml of 2N hydrochloric acid, and the mixture was heated under reflux for one hour. The reaction solution was neutralized with a 2N aqueous solution of sodium hydroxide under ice cooling. Water was added thereto, and the deposited crystals were collected by filtration. The obtained crude crystals were recrystallized from methanol/water to give 291 mg (yield 32%) of Compound 196 as a yellow powder.
Workup
- temperaturethe mixture was heated
- temperatureunder reflux for one hour
- filtrationthe deposited crystals were collected by filtration
- customThe obtained crude crystals
- customwere recrystallized from methanol/water
Sources & evidence
- ORD record
- ord-4f95922336c243b29c29131738b0d39f
- Source dataset
- uspto-grants-1996_01
- Patent number
- US05484920
Reaction notes
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