Hydrochloric Acid → HCID 90218956, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:23]=[C:24]([Cl:26])[CH:25]=1)[CH2:5][O:6][C:7]([NH:9][CH:10]1[CH2:15][CH2:14][N:13](C(OC(C)(C)C)=O)[CH2:12][CH2:11]1)=[O:8].Cl>O1CCOCC1>[NH:13]1[CH2:14][CH2:15][CH:10]([NH:9][C:7](=[O:8])[O:6][CH2:5][C:4]2[CH:3]=[C:2]([Cl:1])[CH:25]=[C:24]([Cl:26])[CH:23]=2)[CH2:11][CH2:12]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A reaction mixture comprising tert-butyl 4-((((3,5-dichlorobenzyl)oxy)carbonyl)amino)piperidine-1-carboxylate (2.01 g, 4.98 mmol) and 4M HCl in dioxane (1.246 ml, 4.98 mmol) in dioxane (16.61 ml) was stirred at room temperature for 1 hour. The resulting mixture was concentrated under reduced pressure. No further purification under taken and the material was dried and taken on to the next step.
Workup
- concentrationThe resulting mixture was concentrated under reduced pressure
- customNo further purification
- customthe material was dried
Sources & evidence
- ORD record
- ord-3e7c472a67d447c1a38f162c6b5b31a9
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09409895B2
Reaction notes
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