1,4-Dioxane hydrochloride → HCID 69697249, compound
Reaction equation
[F:1][C:2]1[CH:7]=[C:6]([CH:8]([C:10]2[CH:14]=[C:13]([N:15]=[C:16]([N:26]3[CH2:31][CH2:30][O:29][CH2:28][CH2:27]3)[N:17]=[C:18]([NH2:25])[N:19]3[CH2:24][CH2:23][O:22][CH2:21][CH2:20]3)[O:12][N:11]=2)[CH3:9])[CH:5]=[CH:4][C:3]=1[C:32]1[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=1.[ClH:38].O1CCOCC1>O1CCOCC1>[ClH:38].[F:1][C:2]1[CH:7]=[C:6]([CH:8]([C:10]2[CH:14]=[C:13]([N:15]=[C:16]([N:26]3[CH2:31][CH2:30][O:29][CH2:28][CH2:27]3)[N:17]=[C:18]([NH2:25])[N:19]3[CH2:24][CH2:23][O:22][CH2:21][CH2:20]3)[O:12][N:11]=2)[CH3:9])[CH:5]=[CH:4][C:3]=1[C:32]1[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The compound (1.66 g) obtained in Example 108 was dissolved in 1,4-dioxane (20 ml) and thereto was added a 4 N hydrogen chloride/1,4-dioxane solution (1.00 ml), after which the resulting mixture was stirred at room temperature for 2 hours, upon which a white precipitate separated. The reaction mixture was heated to 100° C. to dissolve the precipitate and thereafter allowed to slowly cool with stirring. The resulting white precipitate was separated by filtration to obtain the desired compound (1.19 g).
Workup
- customseparated
- temperatureThe reaction mixture was heated to 100° C.
- dissolutionto dissolve the precipitate
- temperatureto slowly cool
- stirringwith stirring
- customThe resulting white precipitate was separated by filtration
Sources & evidence
- ORD record
- ord-83734bc4d1e84cf9bb9012e66707e5a1
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06100260
Reaction notes
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