Water → HCID 73855058, compound

HRID 1242000Notes

Reaction equation

HRID 1242000 reaction equation
[CH2:1]([N:8]1[C:12](=[O:13])[C:11](=[C:14]2[N:18]([CH3:19])[C:17]3[CH:20]=[CH:21][CH:22]=[CH:23][C:16]=3[S:15]2)[S:10][C:9]1=[N:24][C:25]1[CH:26]=[C:27]([NH:34]C(=O)C(F)(F)F)[CH:28]=[CH:29][C:30]=1[NH:31][CH2:32][CH3:33])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O.C([O-])([O-])=O.[K+].[K+]>CO.CCOC(C)=O>[NH2:34][C:27]1[CH:28]=[CH:29][C:30]([NH:31][CH2:32][CH3:33])=[C:25]([N:24]=[C:9]2[N:8]([CH2:1][C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)[C:12](=[O:13])[C:11](=[C:14]3[N:18]([CH3:19])[C:17]4[CH:20]=[CH:21][CH:22]=[CH:23][C:16]=4[S:15]3)[S:10]2)[CH:26]=1

Participants

6

Conditions

Temperature
55 °C

Procedure

To the product of Example 138 (0.15 g, 0.26 mmol) in MeOH (30 mL) was added H2O (6 mL) and fine mesh K2CO3 (0.30 g, 1.5 mmol), and the solution was stirred 24 h at 55° C. The reaction mixture was cooled, diluted with EtOAc (30 mL), washed with H2O (20 mL), dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude material was purified by reverse-phase HPLC (C18 column), eluting with 0.05% TFA in MeCN—H2O (1:9 to 9:1) to provide the title compound (2 mg). MS(ESI): 488(MH+).

Workup

  1. temperatureThe reaction mixture was cooled
  2. washwashed with H2O (20 mL)
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated under reduced pressure
  6. customThe crude material was purified by reverse-phase HPLC (C18 column)
  7. washeluting with 0.05% TFA in MeCN—H2O (1:9 to 9:1)

Sources & evidence

ORD record
ord-eacf9cbc6383454d9adf499947b8344e
Source dataset
uspto-grants-2006_10
Patent number
US07115640B2

Reaction notes

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