Acetyl chloride → 1-[2-(3-Ethyl-5-methyl-1,2-oxazol-4-yl)-1H-indol-3-yl]ethan-1-one

HRID 1156589Notes

Reaction equation

HRID 1156589 reaction equation
[CH2:1]([C:3]1[C:7]([C:8]2[NH:9][C:10]3[C:15]([CH:16]=2)=[CH:14][CH:13]=[CH:12][CH:11]=3)=[C:6]([CH3:17])[O:5][N:4]=1)[CH3:2].[C:18](Cl)(=[O:20])[CH3:19]>FC(F)(F)S([O-])(=O)=O.[Ag+].C(Cl)Cl>[CH2:1]([C:3]1[C:7]([C:8]2[NH:9][C:10]3[C:15]([C:16]=2[C:18](=[O:20])[CH3:19])=[CH:14][CH:13]=[CH:12][CH:11]=3)=[C:6]([CH3:17])[O:5][N:4]=1)[CH3:2]

Participants

5

Procedure

A solution of 33.5 g. (0.148 mole) of 2-(3-ethyl-5-methyl-4-isoxazolyl)-indole in 450 ml. methylene chloride is treated by the portionwise addition of 41.8 g. (0.163 mole) of silver trifluoromethanesulfonate. The resulting suspension is then treated by the dropwise addition of 12.8 g. (0.163 mole) of acetyl chloride in 50 ml. methylene chloride. The temperature rises to 35° C. during the addition. After the addition is complete the mixture is stirred at room temperature for 4 hours and then filtered. The filtrate is washed with 150 ml. 2 N sodium hydroxide, water and 2 N sodium hydroxide dried over anhydrous magnesium sulfate and evaporated in vacuo to give an oil. The oil is crystallized from ether to give 2-(3-ethyl-5-methyl-4-isoxazolyl)-3-acetyl indole, m.p. 170°-173° C.

Workup

  1. additionThe resulting suspension is then treated by the dropwise addition of 12.8 g
  2. additionThe temperature rises to 35° C. during the addition
  3. additionAfter the addition
  4. filtrationfiltered
  5. washThe filtrate is washed with 150 ml
  6. dry with material2 N sodium hydroxide, water and 2 N sodium hydroxide dried over anhydrous magnesium sulfate
  7. customevaporated in vacuo
  8. customto give an oil
  9. customThe oil is crystallized from ether

Sources & evidence

ORD record
ord-744e080346e94b24826948167a2602c7
Source dataset
uspto-grants-1982_06
Patent number
US04336391

Reaction notes

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