HCID 21266135, compound → HCID 21266154, compound
Reaction equation
[ClH:1].C(OCC)(=O)C.[CH3:8][N:9]1[CH2:14][CH2:13][N:12]([C:15]([O:17][CH2:18][CH:19]2[CH:24]([C:25]([NH:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH3:41])=[O:26])[CH2:23][CH:22]=[CH:21][CH2:20]2)=[O:16])[CH2:11][CH2:10]1>C(OCC)(=O)C>[ClH:1].[CH3:8][N:9]1[CH2:10][CH2:11][N:12]([C:15]([O:17][CH2:18][CH:19]2[CH:24]([C:25]([NH:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][CH2:40][CH3:41])=[O:26])[CH2:23][CH:22]=[CH:21][CH2:20]2)=[O:16])[CH2:13][CH2:14]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4N Hydrochloric acid/ethyl acetate solution (1.58 ml) was added to a solution of {6-[(tetradecylamino)carbonyl]-3-cyclohexenyl}methyl 4-methyltetrahydro-1(2H)-pyrazinecarboxylate (2.500 g) in ethyl acetate (25 ml). After being stirred for 30 minutes at room temperature, the reaction mixture was concentrated. The residue was recrystallized with ethyl acetate-ethanol mixed solution, thereby yielding the entitled compound (2.147 g) as white solid.
Workup
- concentrationthe reaction mixture was concentrated
- customThe residue was recrystallized with ethyl acetate-ethanol mixed solution
Sources & evidence
- ORD record
- ord-f11cc42e88b44bc7a8296c3d764664a6
- Source dataset
- uspto-grants-2001_01
- Patent number
- US06174885B1
Reaction notes
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