Hydrochloric Acid → HCID 131730087, compound
Reaction equation
[CH:1]1([CH2:4][C:5]2([C:18]([O:20][CH2:21][CH3:22])=[O:19])[CH2:10][CH2:9][N:8](C(OC(C)(C)C)=O)[CH2:7][CH2:6]2)[CH2:3][CH2:2]1.[ClH:23]>O1CCOCC1>[ClH:23].[CH2:21]([O:20][C:18]([C:5]1([CH2:4][CH:1]2[CH2:2][CH2:3]2)[CH2:6][CH2:7][NH:8][CH2:9][CH2:10]1)=[O:19])[CH3:22]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 0.5 g (1.6 mmol) 1-tert-butyl 4-ethyl 4-(cyclopropylmethyl)piperidine-1,4-dicarboxylate (commercially available) in 20 mL dioxane was treated with 4 mL 4N HCl in dioxane and stirred at room temperature over night. The mixture was evaporated to dryness and used without further purification in the consecutive step.
Workup
- customThe mixture was evaporated to dryness
- customused without further purification in the consecutive step
Sources & evidence
- ORD record
- ord-ee80fb416204499da46591ef2c6d41d2
- Source dataset
- uspto-grants-2012_12
- Patent number
- US08324250B2
Reaction notes
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