Triethylamine → HCID 57860149, compound

HRID 1513600Notes

Reaction equation

HRID 1513600 reaction equation
Cl.[CH3:2][O:3][C:4]1[C:8]2[C:9](=[O:26])[N:10]([CH2:17][C:18](=[O:25])[C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[C:11]3[CH:12]=[CH:13][CH:14]=[CH:15][C:16]=3[C:7]=2[N:6]([CH3:27])[C:5]=1[C:28]([NH:30][CH2:31][CH:32]1[CH2:37][CH2:36][NH:35][CH2:34][CH2:33]1)=[O:29].C(N(CC)CC)C.[C:45]([O:48][CH2:49][C:50](Cl)=[O:51])(=[O:47])[CH3:46]>C1COCC1.C(=O)([O-])O.[Na+]>[C:45]([O:48][CH2:49][C:50]([N:35]1[CH2:34][CH2:33][CH:32]([CH2:31][NH:30][C:28]([C:5]2[N:6]([CH3:27])[C:7]3[C:16]4[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=4[N:10]([CH2:17][C:18](=[O:25])[C:19]4[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=4)[C:9](=[O:26])[C:8]=3[C:4]=2[O:3][CH3:2])=[O:29])[CH2:37][CH2:36]1)=[O:51])(=[O:47])[CH3:46]

Participants

6

Procedure

To a solution of the compound of Example 542 (400 mg, 0.76 mmol) and triethylamine (0.29 mL, 2.1 mmol) in THF (17 mL) was added acetoxyacetyl chloride (0.10 mL, 0.95 mmol) under ice-cooling, and the mixture was stirred at room temperature for 4 hr. The reaction mixture was diluted with saturated aqueous sodium hydrogen carbonate solution, and extracted twice with ethyl acetate. The extract was combined, washed with saturated brine, dried over magnesium sulfate, and filtered through aminosilica gel. The filtrate was concentrated, and the residue was recrystallized from ethanol-hexane to give the title compound (321 mg, 71%) as a white solid.

Workup

  1. temperaturecooling
  2. extractionextracted twice with ethyl acetate
  3. washwashed with saturated brine
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered through aminosilica gel
  6. concentrationThe filtrate was concentrated
  7. customthe residue was recrystallized from ethanol-hexane

Sources & evidence

ORD record
ord-a7db42d05c0a486d8364e71714efe7bb
Source dataset
uspto-grants-2012_07
Patent number
US08217176B2

Reaction notes

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