1,4-Dioxane hydrochloride → HCID 58424943, compound
Reaction equation
[CH3:1][N:2]1[C:11]2[C:10]3[CH:12]=[C:13]([O:16][CH:17]4[CH2:22][CH2:21][N:20](C(OC(C)(C)C)=O)[CH2:19][CH2:18]4)[CH:14]=[CH:15][C:9]=3[NH:8][C:7](=[O:30])[C:6]=2[CH2:5][CH2:4][CH2:3]1.O1CCOCC1.Cl>O1CCOCC1>[CH3:1][N:2]1[C:11]2[C:10]3[CH:12]=[C:13]([O:16][CH:17]4[CH2:18][CH2:19][NH:20][CH2:21][CH2:22]4)[CH:14]=[CH:15][C:9]=3[NH:8][C:7](=[O:30])[C:6]=2[CH2:5][CH2:4][CH2:3]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The compound (70 mg, 0.17 mmol) prepared in step 1 was dissolved in 1,4-dioxane (3 ml), added with 3.7 N hydrochloric acid 1,4-dioxane solution. The resulting mixture was stirred overnight at room temperature and the precipitate was collected by filtration to obtain the title compound (56 mg, yield: 86%, brown solid).
Workup
- filtrationthe precipitate was collected by filtration
Sources & evidence
- ORD record
- ord-5ac26afe3c6045f7a351e0839173491c
- Source dataset
- uspto-grants-2014_08
- Patent number
- US08815891B2
Reaction notes
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