Triethylamine → HCID 12989090, compound

HRID 277168Notes

Reaction equation

HRID 277168 reaction equation
[C@@H:1]12[CH2:9][CH2:8][C:7](=[O:10])[C@@H:6]1[CH2:5][CH2:4][C:3](=[O:11])[NH:2]2.[CH3:12][C:13]1[CH:21]=[CH:20][C:16]([C:17](Cl)=[O:18])=[CH:15][CH:14]=1.C(N(CC)CC)C>ClCCl>[C:13]1([CH3:12])[CH:21]=[CH:20][C:16]([C:17]([N:2]2[C:3](=[O:11])[CH2:4][CH2:5][C@@H:6]3[C@H:1]2[CH2:9][CH2:8][C:7]3=[O:10])=[O:18])=[CH:15][CH:14]=1

Participants

5

Reactant 3

HCID 8471TriethylamineHCID 134054-Methylbenzoyl ChlorideHCID 54441068HCID 54441068, compound

Product 1

HCID 12989090HCID 12989090, compoundYield 66%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

In 20 ml of dichloromethane were dissolved 0.3 g of Compound 6b obtained in Example 11 and 0.39 g of 4-methylbenzoyl chloride. Thereto was added dropwise 0.38 ml of triethylamine with ice cooling. The mixture was reacted at room temperature for 12 hours. The reaction mixture was washed with 0.1N hydrochloric acid, with 0.1N aqueous solution of NaOH and then with water, and dried over anhydrous sodium sulfate. After dried, the solvent was removed and the residue was recrystallized to obtain 0.35 g of Compound mentioned above (yield: 66%). Table 6 shows analytical data.

Workup

  1. customThe mixture was reacted at room temperature for 12 hours
  2. washThe reaction mixture was washed with 0.1N hydrochloric acid, with 0.1N aqueous solution of NaOH
  3. dry with materialwith water, and dried over anhydrous sodium sulfate
  4. customAfter dried
  5. customthe solvent was removed
  6. customthe residue was recrystallized

Sources & evidence

ORD record
ord-d3204d3356624c66a38017c01f67b60e
Source dataset
uspto-grants-2002_03
Patent number
US06355668B1

Reaction notes

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