Sodium Bicarbonate → HCID 67171478, compound

HRID 545252Notes

Reaction equation

HRID 545252 reaction equation
[CH2:1]([N:4]1[C:12](=[O:13])[C:11]2[C:6](=[N:7][C:8]([NH:14][C:15]3[CH:20]=[CH:19][C:18]([N:21]4[CH2:26][CH2:25][N:24]([CH2:27][C:28]([N:30]([CH3:32])[CH3:31])=[O:29])[CH2:23][CH2:22]4)=[CH:17][CH:16]=3)=[N:9][CH:10]=2)[N:5]1[C:33]1[CH:38]=[CH:37][CH:36]=[C:35]([C:39](O)([CH3:41])[CH3:40])[N:34]=1)[CH:2]=[CH2:3].COCCN(S(F)(F)[F:53])CCOC.C(=O)([O-])O.[Na+]>C(Cl)(Cl)Cl>[CH2:1]([N:4]1[C:12](=[O:13])[C:11]2[C:6](=[N:7][C:8]([NH:14][C:15]3[CH:20]=[CH:19][C:18]([N:21]4[CH2:26][CH2:25][N:24]([CH2:27][C:28]([N:30]([CH3:32])[CH3:31])=[O:29])[CH2:23][CH2:22]4)=[CH:17][CH:16]=3)=[N:9][CH:10]=2)[N:5]1[C:33]1[CH:38]=[CH:37][CH:36]=[C:35]([C:39]([F:53])([CH3:41])[CH3:40])[N:34]=1)[CH:2]=[CH2:3]

Participants

5

Procedure

16 mg of the compound obtained in Example 92 was dissolved in 3 mL of chloroform, and 0.1 mL of bis(2-methoxyethyl)aminosulfur trifluoride was added thereto and stirred at room temperature for 1 hour. Aqueous saturated sodium hydrogencarbonate solution was added to it and extracted with chloroform. The chloroform layer was washed with saturated saline water, dried with anhydrous sodium sulfate, and the solvent was evaporated away under reduced pressure. This was purified through column chromatography (ethyl acetate/chloroform=3/1) and then solidified from ethyl acetate/hexane solution to obtain 8 mg of the entitled compound as a yellow solid.

Workup

  1. extractionextracted with chloroform
  2. washThe chloroform layer was washed with saturated saline water
  3. dry with materialdried with anhydrous sodium sulfate
  4. customthe solvent was evaporated away under reduced pressure
  5. customThis was purified through column chromatography (ethyl acetate/chloroform=3/1)

Sources & evidence

ORD record
ord-cb56260071dd44f993069d5dc86b5850
Source dataset
uspto-grants-2011_05
Patent number
US07935708B2

Reaction notes

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