Hydrochloric Acid → HCID 25143778, compound

HRID 2199717Notes

Reaction equation

HRID 2199717 reaction equation
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([O:12][CH2:13][CH2:14][CH2:15][C:16]2[C:24]3[C:19](=[C:20]([C:25]4[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=4[O:31][CH3:32])[CH:21]=[CH:22][CH:23]=3)[NH:18][C:17]=2[C:33]([O:35]CC)=[O:34])=[CH:4][CH:3]=1.O[Li].O.Cl>C1COCC1.CO.O>[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5]([O:12][CH2:13][CH2:14][CH2:15][C:16]2[C:24]3[C:19](=[C:20]([C:25]4[CH:30]=[CH:29][CH:28]=[CH:27][C:26]=4[O:31][CH3:32])[CH:21]=[CH:22][CH:23]=3)[NH:18][C:17]=2[C:33]([OH:35])=[O:34])=[CH:4][CH:3]=1

Participants

7

Procedure

A mixture of EXAMPLE 65A (70 mg) in THF (2 mL), methanol (1 mL) and water (1 mL) was treated with LiOH.H2O (100 mg) and stirred at ambient temperature overnight. The mixture was acidified with 5% aqueous HCl and extracted with ethyl acetate. The extract was washed with water, brine and dried (Na2SO4), filtered and concentrated. The concentrate was dissolved in 1:1DMSO/methanol and purified by reverse phase HPLC (C18, 20 to 100% acetonitrile/water/0.1% TFA). 1H NMR (300 MHz, CDCl3) δ 8.72 (s, 1H), 8.38 (dd, 1H), 8.15 (dd, 1H), 7.72 (d, 1H), 7.35-7.57 (m, 5H), 7.08-7.21 (m, 3H), 6.65 (d, 1H), 4.18 (t, 2H), 3.82 (s, 3H), 3.47 (t, 2H), 2.37 (m, 2H).

Workup

  1. extractionextracted with ethyl acetate
  2. washThe extract was washed with water, brine
  3. dry with materialdried (Na2SO4)
  4. filtrationfiltered
  5. concentrationconcentrated
  6. dissolutionThe concentrate was dissolved in 1:1DMSO/methanol
  7. custompurified by reverse phase HPLC (C18, 20 to 100% acetonitrile/water/0.1% TFA)

Sources & evidence

ORD record
ord-ecb2db1e17ef4c669a7d4098dd0c3d61
Source dataset
uspto-grants-2016_06
Patent number
US09359296B2

Reaction notes

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