Hydrochloric Acid → HCID 67246066, compound
Reaction equation
[CH3:1][C@H:2]1[NH:7][C@@H:6]([CH3:8])[CH2:5][N:4]([CH2:9][C:10]2[CH:14]=[CH:13][N:12]([C:15]3[C:16]([N:21]4[CH2:26][CH2:25][CH:24]([NH:27][C:28]5[CH:33]=[CH:32][C:31]([F:34])=[CH:30][CH:29]=5)[CH2:23][CH2:22]4)=[N:17][CH:18]=[CH:19][CH:20]=3)[N:11]=2)[CH2:3]1.[ClH:35].C(OCC)C>C(Cl)Cl>[ClH:35].[CH3:1][C@H:2]1[NH:7][C@@H:6]([CH3:8])[CH2:5][N:4]([CH2:9][C:10]2[CH:14]=[CH:13][N:12]([C:15]3[C:16]([N:21]4[CH2:22][CH2:23][CH:24]([NH:27][C:28]5[CH:33]=[CH:32][C:31]([F:34])=[CH:30][CH:29]=5)[CH2:25][CH2:26]4)=[N:17][CH:18]=[CH:19][CH:20]=3)[N:11]=2)[CH2:3]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
E1 (0.42 g, 0.91 mmol) was taken up in DCM (10 ml) and 1.2M HCl in diethylether (0.76 ml, 0.91 mmol) was added. Removal of the solvent in vacuo yielded the title compound as a yellow solid (0.45 g), δH (DMSO-d6) 1.08 (6H, d), 1.83 (2H, d), 2.07 (2H, br t), 2.72 (2H, t), 2.95 (2H, br d), 3.16 (2H, d), 3.25 (3H, br s), 3.64 (2H, s), 5.38 (1H, br d), 6.45 (1H, s), 6.56 (2H, br s), 6.88 (2H, t), 7.03 (1H, m), 7.69 (1H, d), 8.12 (1H, s), 8.26 (2H, m), 9.09 (1H, br s).
Workup
- customRemoval of the solvent in vacuo
Sources & evidence
- ORD record
- ord-bbc6d2da7a1f41f592d9d69bd6076907
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07964602B2
Reaction notes
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