Triethylamine → HCID 25009727, compound

HRID 547514Notes

Reaction equation

HRID 547514 reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][CH2:9][C:10]([NH:12][C:13]2[C:14]([C:26]([OH:28])=O)=[N:15][N:16]([CH2:18][CH2:19][C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[CH:17]=2)=[O:11])=[CH:4][CH:3]=1.C(=O)([O-])[O-].[CH2:33]([N:35](CC)CC)[CH3:34].ClCCN>O1CCCC1.CN(C1C=CC=CN=1)C>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([S:8][CH2:9][C:10]([NH:12][C:13]2[C:14]([C:26]3[O:28][CH2:34][CH2:33][N:35]=3)=[N:15][N:16]([CH2:18][CH2:19][C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[CH:17]=2)=[O:11])=[CH:6][CH:7]=1

Participants

7

Reactant 4

HCID 8471TriethylamineHCID 133692-ChloroethylamineHCID 19660Carbonate IonHCID 25009726KR-33494

Product 1

HCID 25009727HCID 25009727, compoundYield 99%

Reagents, catalysts & solvents 2

HCID 218852-DimethylaminopyridineCatalystHCID 8028TetrahydrofuranSolvent

Procedure

380 mg (0.83 mM) of the compound obtained in Example 23 was dissolved in 1 ml of tetrahydrofuran to which 356 mg (1.65 mM) of di(2-pyridyl (0.1 equivalent)) carbonate and 10 mg (0.08 mM) of dimethylaminopyridine were added dropwise, and the resulting mixture was stirred under a nitrogen atmosphere for 30 minutes. Subsequently, 0.17 ml (1.20 mM) of triethylamine and 144 mg (1.20 mM) of 2-chloroethylamine were added thereto, and the resulting mixture was stirred under a nitrogen atmosphere for 1 hour. The solvent was distilled off under reduced pressure, and the resultant was extracted with ethyl acetate and brine. The organic solvent layer was dried over anhydrous sodium sulfate, filtered, and then distilled under reduced pressure. The resulting impure compound was purified by column chromatography (hexane:ethyl acetate=2:1), to obtain 426 mg (99%) of the title compound.

Workup

  1. additionwere added dropwise
  2. stirringthe resulting mixture was stirred under a nitrogen atmosphere for 1 hour
  3. distillationThe solvent was distilled off under reduced pressure
  4. extractionthe resultant was extracted with ethyl acetate and brine
  5. dry with materialThe organic solvent layer was dried over anhydrous sodium sulfate
  6. filtrationfiltered
  7. distillationdistilled under reduced pressure
  8. customThe resulting impure compound was purified by column chromatography (hexane:ethyl acetate=2:1)

Sources & evidence

ORD record
ord-f8b80ddd4c064fcfb5bd5a6a404d285e
Source dataset
uspto-grants-2011_05
Patent number
US07939550B2

Reaction notes

Loading…