1,4-Dioxane hydrochloride → HCID 58424899, compound
Reaction equation
C(=O)([O:7][C:8]1[CH:25]=[CH:24][C:11]2[N:12]([CH2:21][O:22][CH3:23])[C:13](=[O:20])[C:14]3[CH:15]=[CH:16][CH:17]=[N:18][C:19]=3[C:10]=2[CH:9]=1)OC(C)(C)C.O1CCOCC1.Cl>O1CCOCC1>[OH:7][C:8]1[CH:25]=[CH:24][C:11]2[N:12]([CH2:21][O:22][CH3:23])[C:13](=[O:20])[C:14]3[CH:15]=[CH:16][CH:17]=[N:18][C:19]=3[C:10]=2[CH:9]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The compound (580 mg, 1.627 mmol) prepared in step 4 was dissolved in 1,4-dioxane (10 ml), added with 3.7 N hydrochloric acid 1,4-dioxane solution (6 ml). The resulting mixture was stirred for one day at room temperature and the precipitate was collected by filtration to obtain the title compound (410 mg, yield: 98%, yellow solid).
Workup
- filtrationthe precipitate was collected by filtration
Sources & evidence
- ORD record
- ord-af727358b3dd4ae281f56978880208a7
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08815891B2
Reaction notes
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