Hydrochloric Acid → HCID 67812950, compound

HRID 1024661Notes

Reaction equation

HRID 1024661 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

5

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

  1. concentrationThe colorless solution was concentrated in vacuo
  2. 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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