Hydrochloric Acid → HCID 67559449, compound
Reaction equation
C(OC([N:8]1[CH2:13][CH2:12][C:11]([C:24]#[N:25])([C:14]2[CH:23]=[CH:22][C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH:15]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:26].O1CCOCC1>>[ClH:26].[C:24]([C:11]1([C:14]2[CH:23]=[CH:22][C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH:15]=2)[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]1)#[N:25]Participants
4
Procedure
Combine 1-tert-butoxycarbonyl-4-cyano-4-(naphth-2-yl)-piperidine (3.12 mmol) and HCl in dioxane (10 mL, 40 mmol, 4N, 13 eq.) at ambient temperature for 1 h. Concentrate the solvent in vacuo and dry under high vacuum to give the title compound.
Workup
- concentrationConcentrate the solvent in vacuo
- customdry under high vacuum
Sources & evidence
- ORD record
- ord-9272606a1ff940b59d09c3d62c202009
- Source dataset
- uspto-grants-1997_06
- Patent number
- US05635510
Reaction notes
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