Ethyl formate → HCID 15029813, compound

HRID 1534033Notes

Reaction equation

HRID 1534033 reaction equation
Cl.[O:2]([C:4]1[CH:13]=[CH:12][CH:11]=[C:10]2[C:5]=1[CH2:6][CH2:7][CH2:8][CH:9]2[CH2:14][NH2:15])[CH3:3].[CH:16](OCC)=[O:17]>C1(C)C=CC=CC=1>[CH:16]([NH:15][CH2:14][CH:9]1[C:10]2[C:5](=[C:4]([O:2][CH3:3])[CH:13]=[CH:12][CH:11]=2)[CH2:6][CH2:7][CH2:8]1)=[O:17]

Participants

4

Reactant 2

HCID 8025Ethyl formateHCID 19098380HCID 19098380, compound

Product 1

HCID 15029813HCID 15029813, compound

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

The product from Example 14 was converted to its free base (3.4 g) and dissolved into toluene (30 ml). Ethyl formate (5 ml) was added and the reaction stirred at reflux for 5 hr. The solvent was removed to afford a solid. Recrystallization from Et2O/CH2Cl2 afforded 3.07 g of desired product. Anal. calcd. for C13H17NO2 ; C, 71.21; H, 7.81; N, 6.39. Found: C, 71.26; H, 7.82; N, 6.41.

Workup

  1. temperatureat reflux for 5 hr
  2. customThe solvent was removed
  3. customto afford a solid
  4. customRecrystallization from Et2O/CH2Cl2

Sources & evidence

ORD record
ord-240bde6631444072abe5dc05a40ae96d
Source dataset
uspto-grants-1992_02
Patent number
US05086074

Reaction notes

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