Hydrochloric Acid → HCID 68831865, compound
Reaction equation
[Cl:1][C:2]1[CH:45]=[CH:44][C:5]([CH2:6][C@H:7]([C:20]([N:22]2[CH:27]3[CH2:28][CH2:29][CH:23]2[CH2:24][CH:25]([N:30]([CH:38]2[CH2:43][CH2:42][CH2:41][CH2:40][CH2:39]2)[C:31]([N:33]([CH2:36][CH3:37])[CH2:34][CH3:35])=[O:32])[CH2:26]3)=[O:21])[NH:8][CH2:9][C@H:10]2[CH2:19][C:18]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[CH2:12][NH:11]2)=[CH:4][CH:3]=1.Cl>ClCCl.O1CCOCC1>[ClH:1].[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:6][C@H:7]([C:20]([N:22]2[CH:23]3[CH2:29][CH2:28][CH:27]2[CH2:26][CH:25]([N:30]([CH:38]2[CH2:43][CH2:42][CH2:41][CH2:40][CH2:39]2)[C:31]([N:33]([CH2:34][CH3:35])[CH2:36][CH3:37])=[O:32])[CH2:24]3)=[O:21])[NH:8][CH2:9][C@H:10]2[CH2:19][C:18]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[CH2:12][NH:11]2)=[CH:44][CH:45]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
0.12 g of N-(8-{4-chloro-N-[(3R)-1,2,3,4-tetrahydroisoquinolin-3-ylmethyl]-D-phenylalanyl}-8-azabicyclo[3.2.1]oct-3-yl)-N-cyclohexyl-N′,N′-diethylurea is dissolved in 5 ml of dichloromethane and 0.4 ml of 4N hydrochloric acid in dioxane is added. After evaporation, the residue is taken up in diethyl ether, rinsing is carried out with diethyl ether and the precipitate obtained is filter-dried. 0.12 g of N-(8-{4-chloro-N-[(3R)-1,2,3,4-tetrahydroisoquinolin-3-ylmethyl]-D-phenylalanyl}-8-azabicyclo[3.2.1]oct-3-yl)-N-cyclohexyl-N′,N′-diethylurea hydrochloride is obtained.
Workup
- customAfter evaporation
- washrinsing
- customthe precipitate obtained
- customis filter-dried
Sources & evidence
- ORD record
- ord-398c8f0ddbf647a3a51fd442f5aeaf94
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07569582B2
Reaction notes
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