Benzoylacetone → HCID 10737736, compound

HRID 1251489Notes

Reaction equation

HRID 1251489 reaction equation
[Br:1][C:2]1[CH:7]=[C:6]([CH:8]([CH3:10])[CH3:9])[CH:5]=[CH:4][C:3]=1[N:11]1[C:19]2[C:14](=[C:15]([CH3:21])[CH:16]=[C:17]([CH3:20])[N:18]=2)[C:13]([C:22]#[N:23])=[CH:12]1.[C:24]([CH2:32][C:33](=O)C)(=O)[C:25]1C=CC=C[CH:26]=1.C1(C)C(C)=CC=CC=1>O>[Br:1][C:2]1[CH:7]=[C:6]([CH:8]([CH3:10])[CH3:9])[CH:5]=[CH:4][C:3]=1[N:11]1[C:19]2[C:14](=[C:15]([CH3:21])[CH:16]=[C:17]([C:20]3[CH:33]=[CH:32][CH:24]=[CH:25][CH:26]=3)[N:18]=2)[C:13]([C:22]#[N:23])=[CH:12]1.[Br:1][C:2]1[CH:7]=[C:6]([CH:8]([CH3:10])[CH3:9])[CH:5]=[CH:4][C:3]=1[N:11]1[C:19]2[C:14](=[C:15]([CH3:21])[CH:16]=[C:17]([CH3:20])[N:18]=2)[C:13]([C:22]#[N:23])=[CH:12]1

Participants

6

Procedure

A mixture of 737 mg (2.00 mmole) of the product from Example 64 (Part B), 324 mg (2.00 mmole) of benzoylacetone and 25 mL of xylene was heated in a flask equipped with a water separator for 2 hours. The solvent was removed by evaporation, and the residue chromatographed on silica gel, eluting in step gradients with 0, 5, 10; and 15% ethyl acetate in hexane. Both 1-(2-bromo-4-isopropylphenyl)-3-cyano-4-methyl-6-phenyl-7-azaindole and 1-(2-bromo-4-isopropylphenyl)-3-cyano-6-methyl-4-methyl-7-azaindole were obtained. The Rf values were respectively 0.38 and 0.28 (silica gel with 80:20 hexane-ethyl acetate). The assignment of the structures was based on the nmr data of the de-cyanylated compounds in Example 67.

Workup

  1. temperaturewas heated in a flask
  2. customThe solvent was removed by evaporation
  3. customthe residue chromatographed on silica gel
  4. washeluting in step gradients with 0, 5, 10

Sources & evidence

ORD record
ord-c9c916bedd854f2ea3b2e2d9b6ad802f
Source dataset
uspto-grants-2002_01
Patent number
US06342503B1

Reaction notes

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