Hydrochloric Acid → HCID 25099970, compound

HRID 533253Notes

Reaction equation

HRID 533253 reaction equation
[CH3:1][O:2][C:3]1[CH:37]=[CH:36][C:6]([CH2:7][N:8]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[C:10]([O:17][CH2:18][CH2:19][O:20][C:21]3[C:30]4[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=4)[CH:24]=[CH:23][CH:22]=3)=[C:9]2[C:31]([O:33]CC)=[O:32])=[CH:5][CH:4]=1.[Li+].[OH-].Cl>O1CCCC1.CO.O>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:7][N:8]2[C:16]3[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=3)[C:10]([O:17][CH2:18][CH2:19][O:20][C:21]3[C:30]4[C:25](=[CH:26][CH:27]=[CH:28][CH:29]=4)[CH:24]=[CH:23][CH:22]=3)=[C:9]2[C:31]([OH:33])=[O:32])=[CH:36][CH:37]=1

Participants

7

Procedure

To a solution of EXAMPLE 101C (80 mg) in tetrahydrofuran (2 ml), methanol (1 ml) and water (1 ml) was added LiOH (100 mg). The mixture was stirred at room temperature overnight. The mixture was then acidified with 5% HCl and extracted with ethyl acetate (200 ml). The organic layer was washed with water, brine and dried over Na2SO4. After concentration of the solvent, the residue was dissolved in DMSO/methanol (1:1, 1.5 ml) and purified via reverse phaseHPLC. 1H NMR (500 MHz, dimethyl sulfoxide-d6) δ 12.99 (m, 1H), 8.01 (m, 1H), 7.86 (m, 1H), 7.73 (m, 1H), 7.46 (m, 6H), 7.27 (m, 1H), 6.98 (m, 3H), 6.74 (m, 2H), 5.70 (s, 2H), 4.64 (m, 2H), 4.48 (m, 2H), 3.67 (s, 3H).

Workup

  1. extractionextracted with ethyl acetate (200 ml)
  2. washThe organic layer was washed with water, brine
  3. dry with materialdried over Na2SO4
  4. dissolutionAfter concentration of the solvent, the residue was dissolved in DMSO/methanol (1:1, 1.5 ml)
  5. custompurified via reverse phaseHPLC

Sources & evidence

ORD record
ord-1e57077813214296ad9818673f60ee9f
Source dataset
uspto-grants-2014_10
Patent number
US08853209B2

Reaction notes

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