Hydrochloric Acid → HCID 9808299, compound
Reaction equation
Cl.[CH3:2][O:3][C:4](=[O:37])[CH2:5][CH2:6][C:7]([N:9]1[C:17]2[C:12](=[CH:13][C:14]([CH2:19][CH2:20][N:21]3[CH2:26][CH2:25][N:24]([C:27]4[C:31]5[CH:32]=[CH:33][CH:34]=[CH:35][C:30]=5[S:29][N:28]=4)[CH2:23][CH2:22]3)=[C:15]([Cl:18])[CH:16]=2)[CH2:11][C:10]1=[O:36])=[O:8].[CH2:38](O)C.Cl>O>[ClH:18].[CH2:2]([O:3][C:4](=[O:37])[CH2:5][CH2:6][C:7]([N:9]1[C:17]2[C:12](=[CH:13][C:14]([CH2:19][CH2:20][N:21]3[CH2:26][CH2:25][N:24]([C:27]4[C:31]5[CH:32]=[CH:33][CH:34]=[CH:35][C:30]=5[S:29][N:28]=4)[CH2:23][CH2:22]3)=[C:15]([Cl:18])[CH:16]=2)[CH2:11][C:10]1=[O:36])=[O:8])[CH3:38]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The product of Example 5, (611 mg, 1.1 mmol) was mixed with ethanol (27 mL) and concentrated hydrochloric acid (0.5 mL) and the mixture boiled under reflux for 24 h in the temperature range 78-80° C. Distilled water (20 mL) was added to the hot reaction mixture and solids removed during the hot filtration. The filtrate was cooled further and product solids were isolated by filtration, washed with distilled water (20 mL), and dried under vacuum to yield 200 mg (32%).
Workup
- temperatureunder reflux for 24 h in the temperature
- customrange 78-80° C
- customremoved during the hot filtration
- temperatureThe filtrate was cooled further
- customproduct solids were isolated by filtration
- washwashed with distilled water (20 mL)
- customdried under vacuum
- customto yield 200 mg (32%)
Sources & evidence
- ORD record
- ord-819d2298957f449883c03c4ac753f127
- Source dataset
- uspto-grants-2006_03
- Patent number
- US07019009B2
Reaction notes
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