Hydrochloric Acid → HCID 66986037, compound
Reaction equation
[C:1]([C:5]1[CH:6]=[C:7]([NH:21][C:22]([C:24]2[N:25]([CH3:48])[C:26]3[C:31]([CH:32]=2)=[CH:30][CH:29]=[CH:28][C:27]=3[CH2:33][N:34]2[CH2:39][CH2:38][N:37]([C:40]([CH:42]3[CH2:46][CH2:45][CH2:44][N:43]3[CH3:47])=[O:41])[CH2:36][CH2:35]2)=[O:23])[C:8]([O:19][CH3:20])=[C:9]([NH:11]C(=O)OC(C)(C)C)[CH:10]=1)([CH3:4])([CH3:3])[CH3:2].[ClH:49]>ClCCl.C(O)(C)C>[ClH:49].[ClH:49].[ClH:49].[NH2:11][C:9]1[C:8]([O:19][CH3:20])=[C:7]([NH:21][C:22]([C:24]2[N:25]([CH3:48])[C:26]3[C:31]([CH:32]=2)=[CH:30][CH:29]=[CH:28][C:27]=3[CH2:33][N:34]2[CH2:35][CH2:36][N:37]([C:40]([C@@H:42]3[CH2:46][CH2:45][CH2:44][N:43]3[CH3:47])=[O:41])[CH2:38][CH2:39]2)=[O:23])[CH:6]=[C:5]([C:1]([CH3:2])([CH3:3])[CH3:4])[CH:10]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
1.59 g tert-butyl [5-tert-butyl-2-methoxy-3-({1-methyl-7-[4-(1-methyl-pyrrolidine-2-carbonyl)-piperazin-1-ylmethyl]-1H-indole-2-carbonyl}-amino)-phenyl]-carbamate are dissolved in 15 ml dichloromethane, combined with 10 ml of a 5 M solution of hydrogen chloride in isopropanol and stirred for 3 hours at ambient temperature. Then the solvents are eliminated in vacuo. The product thus obtained is further reacted directly.
Workup
- customThe product thus obtained
- customis further reacted directly
Sources & evidence
- ORD record
- ord-10f45afe418a485398b96817618349de
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08686022B2
Reaction notes
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