HCID 86738432, compound → 2-(5-Methyl-3-phenyl-1,2-oxazol-4-yl)-1H-indole

HRID 1156573Notes

Reaction equation

HRID 1156573 reaction equation
C1(N[N:8]=[C:9]([C:11]2[C:12]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)=[N:13][O:14][C:15]=2[CH3:16])[CH3:10])C=CC=CC=1>O>[CH3:16][C:15]1[O:14][N:13]=[C:12]([C:17]2[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=2)[C:11]=1[C:9]1[NH:8][C:17]2[C:22]([CH:10]=1)=[CH:21][CH:20]=[CH:19][CH:18]=2

Participants

3

Procedure

To 1350 grams of polyphosphoric acid at 100° to 110° C., there is added portionwise 89.3 g. (0.307 mole) of 1-(5-methyl-3-phenyl-4-isoxazolyl)-1-ethanone phenyl hydrazone, while maintaining the temperature between 105° and 115° C. After addition is complete the mixture is stirred at 100° to 110° C. for 3 hours. The mixture is then poured onto ice and water and the resulting solid is filtered and washed with water. The solid is then dissolved in ether, washed with water, dried and evaporated partially and cooled in ice. The resulting solid is filtered and washed with cold ether to give 2-(5-methyl-3-phenyl-4-isoxazolyl)-indole; m.p. 145° to 146° C.

Workup

  1. additionAfter addition
  2. filtrationthe resulting solid is filtered
  3. washwashed with water
  4. dissolutionThe solid is then dissolved in ether
  5. washwashed with water
  6. customdried
  7. customevaporated partially
  8. temperaturecooled in ice
  9. filtrationThe resulting solid is filtered
  10. washwashed with cold ether

Sources & evidence

ORD record
ord-a45571e7d1f541ca840d3dd8a10fee53
Source dataset
uspto-grants-1982_06
Patent number
US04336378

Reaction notes

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