Hydrochloric Acid → HCID 67562162, compound
Reaction equation
C(OC([N:8]1[CH2:13][CH2:12][C:11]([C:20]#[N:21])([C:14]2[CH:19]=[CH:18][N:17]=[CH:16][CH:15]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:22].O1CCOCC1>>[ClH:22].[C:20]([C:11]1([C:14]2[CH:19]=[CH:18][N:17]=[CH:16][CH:15]=2)[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]1)#[N:21]Participants
4
Procedure
Prepare by the method of example 30.3 using 1-tert-butoxycarbonyl-4-cyano-4-(pyridin-4-yl)-piperidine (3 mmol) and HCl in dioxane (40 mmol, 4N). 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-04df1e0b19b54b618ce5e461f2ef70ca
- Source dataset
- uspto-grants-1997_06
- Patent number
- US05635510
Reaction notes
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