Hydrochloric Acid → HCID 67561003, compound
Reaction equation
C(OC([N:8]1[CH2:13][CH2:12][C:11]([C:19]#[N:20])([C:14]2[S:15][CH:16]=[CH:17][CH:18]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:21].O1CCOCC1>>[ClH:21].[C:19]([C:11]1([C:14]2[S:15][CH:16]=[CH:17][CH:18]=2)[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]1)#[N:20]Participants
4
Procedure
Prepare by the method of example 30.3 using 1-tert-butoxycarbonyl-4-cyano-4-(thiophen-2-yl)-piperidine (3 mmol) and HCl in dioxane (4N, 40 mmol). 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-587daab604bf4bf8b868b3ddd982ce88
- Source dataset
- uspto-grants-1997_06
- Patent number
- US05635510
Reaction notes
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