Hydrochloric Acid → HCID 68457989, compound

HRID 1455785Notes

Reaction equation

HRID 1455785 reaction equation
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([S:15][C:16]2[CH:21]=[CH:20][C:19]([CH2:22][CH2:23][CH2:24][C:25]3([CH2:31]C#N)[CH2:29][O:28]C(=O)[NH:26]3)=[C:18]([Cl:34])[CH:17]=2)[CH:12]=[CH:13][CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-:35].[Na+].Cl.[CH2:38]([OH:40])C>>[ClH:34].[NH2:26][C:25]([CH2:29][OH:28])([CH2:24][CH2:23][CH2:22][C:19]1[CH:20]=[CH:21][C:16]([S:15][C:11]2[CH:12]=[CH:13][CH:14]=[C:9]([O:8][CH2:1][C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)[CH:10]=2)=[CH:17][C:18]=1[Cl:34])[CH2:31][C:38]([OH:40])=[O:35]

Participants

5

Procedure

To the compound of Example 146 (196 mg), a 3 mol/L aqueous solution of sodium hydroxide (5 mL) and ethanol (0.5 mL) were added and the mixture was refluxed for 8 hours. While the mixture was stirred in an ice bath, 4 mol/L hydrochloric acid was added to adjust the pH of the mixture to 2 to 1. Using ethyl acetate and water, the mixture was separated into an organic phase and an aqueous phase. The organic layer was dried over anhydrous sodium sulfate, was concentrated, and was dried in a vacuum pump to give the desired product as a pale white solid (201 mg).

Workup

  1. temperaturethe mixture was refluxed for 8 hours
  2. customUsing ethyl acetate and water, the mixture was separated into an organic phase
  3. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  4. concentrationwas concentrated
  5. customwas dried in a vacuum pump

Sources & evidence

ORD record
ord-425085efa5314ba38ab7eedf21f89417
Source dataset
uspto-grants-2009_01
Patent number
US07482491B2

Reaction notes

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