Dimethylformamide → HCID 67241608, compound

HRID 2357166Notes

Reaction equation

HRID 2357166 reaction equation
Br[C:2]1[CH:3]=[C:4]2[C:12](=[CH:13][CH:14]=1)N(C)[C:10]1[C:9]3[CH:16]=C[CH:18]=[CH:19][C:8]=3[S:7][CH2:6][C:5]2=1.[C:20]([Cu])#[N:21].[CH3:23][N:24]([CH:26]=O)C>>[CH3:16][CH:9]1[C:10]2[C:23]3[N:24]=[CH:26][CH:18]=[CH:19][C:8]=3[S:7][CH2:6][C:5]=2[C:4]2[C:12]1=[CH:13][CH:14]=[C:2]([C:20]#[N:21])[CH:3]=2

Participants

4

Reactant 3

HCID 6228DimethylformamideHCID 44411761HCID 44411761, compoundHCID 178418546HCID 178418546, compound

Product 1

HCID 67241608HCID 67241608, compound

Conditions

Temperature
170 °C

Procedure

A mixture of 8-bromo-11-methyl-6,11-dihydro-5-thia-11-aza-benzo[a]fluorene (270 mg), as prepared in Example 57, and CuCN (270 mg) in DMF (25 ml) was reflux overnight at 170° C. The reaction mixture was filtered through a pad of Celite and then partitioned between saturated NaHCO3 aqueous solution and EtOAc. The aqueous layer was extracted with EtOAc, the organic layers were dried and concentrated to yield crude product. The crude product was purified by chromatography (Hexane:ethyl acetate=5:1) to yield the title compound as a white solid.

Workup

  1. filtrationThe reaction mixture was filtered through a pad of Celite
  2. custompartitioned between saturated NaHCO3 aqueous solution and EtOAc
  3. extractionThe aqueous layer was extracted with EtOAc
  4. customthe organic layers were dried
  5. concentrationconcentrated
  6. customto yield crude product
  7. customThe crude product was purified by chromatography (Hexane:ethyl acetate=5:1)

Sources & evidence

ORD record
ord-df8fcbb223dd46d0ba374e5bf5c0c62d
Source dataset
uspto-grants-2010_07
Patent number
US07759498B2

Reaction notes

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