Hydrochloric Acid → HCID 67812950, compound
Reaction equation
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12]([NH:14][CH2:15][CH2:16][CH2:17][N:18]([CH2:20][C@@H:21]2[C@@H:25]([OH:26])[C@@H:24]([OH:27])[C@H:23]([N:28]3[C:32]4[N:33]=[CH:34][N:35]=[C:36]([NH:37][CH2:38][C:39]5[CH:44]=[CH:43][C:42]([O:45][CH3:46])=[CH:41][C:40]=5[O:47][CH3:48])[C:31]=4[CH:30]=[CH:29]3)[O:22]2)[CH3:19])=[O:13])=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2].[ClH:49].O>CO>[ClH:49].[C:1]([C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12]([NH:14][CH2:15][CH2:16][CH2:17][N:18]([CH2:20][C@@H:21]2[C@@H:25]([OH:26])[C@@H:24]([OH:27])[C@H:23]([N:28]3[C:32]4[N:33]=[CH:34][N:35]=[C:36]([NH:37][CH2:38][C:39]5[CH:44]=[CH:43][C:42]([O:45][CH3:46])=[CH:41][C:40]=5[O:47][CH3:48])[C:31]=4[CH:30]=[CH:29]3)[O:22]2)[CH3:19])=[O:13])=[CH:7][CH:6]=1)([CH3:4])([CH3:2])[CH3:3]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 1-(4-(tert-butyl)phenyl)-3-(3-((((2R,3S,4R,5R)-5-(4-((2,4-dimethoxybenzyl)amino)-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-3,4-dihydroxytetrahydrofuran-2-yl)methyl)(methyl)amino)propyl)urea (20 mg, 0.039 mmol) in methanol (0.7 mL) was added to a mixture of 0.1N HCl (0.39 mL, 0.039 mmol) and water (2.0 mL). The colorless solution was concentrated in vacuo to remove the methanol. The solution was lyophilized to yield the title compound (20 mg, 93%) as a white solid: 1H NMR (400 MHz, D2O) ppm 8.02 (s, 1H), 7.33 (d, 1=3.73 Hz, 1H), 7.21 (d, J=8.09 Hz, 2H), 6.90 (d, J=8.09 Hz, 2H), 6.69 (d, J=3.73 Hz, 1H), 6.13 (d, J=4.56 Hz, 1H), 4.47 (m, 2H), 4.24 (t, J=5.39 Hz, 1H), 3.67 (m, 1H), 3.54 (d, J=12.02 Hz, 1H), 3.33 (m, 1H), 3.22 (m, 1H), 3.11 (m, 1H), 2.94 (s, 3H), 1.90 (m, 2H), 1.20 (s, 9H); MS (ESI+) for C26H37N7O4 m/z 512.3 (M+H)+; (ESI−) for C26H37N7O4 m/z 510.2 (M−H)−; HPLC purity 97% (ret. time, 2.82 min). IC50<10 nM.
Workup
- concentrationThe colorless solution was concentrated in vacuo
- customto remove the methanol
Sources & evidence
- ORD record
- ord-dc1d56faabb844ea885d533b16e50190
- Source dataset
- uspto-grants-2014_05
- Patent number
- US08722877B2
Reaction notes
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