Dimethylformamide → HCID 59654766, compound

HRID 2053104Notes

Reaction equation

HRID 2053104 reaction equation
[C:1]1([C:7]2[O:11][C:10]([C:12]([OH:14])=O)=[CH:9][CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:15]([O:18][C:19]1C=CC(N)=C[C:20]=1CC)(=[O:17])[CH3:16].F[P-](F)(F)(F)(F)F.N1(OC(N(C)C)=[N+](C)C)[C:39]2[N:40]=[CH:41][CH:42]=[CH:43][C:38]=2N=N1.[CH3:52]N(C)C=O>>[CH2:19]([O:18][C:15](=[O:17])[CH2:16][C:38]1[CH:39]=[CH:52][C:41]([NH:40][C:12]([C:10]2[O:11][C:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)=[CH:8][CH:9]=2)=[O:14])=[CH:42][CH:43]=1)[CH3:20]

Participants

5

Reactant 4

HCID 6228DimethylformamideHCID 7362555-Phenylfuran-2-carboxylic acidHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 53958485HCID 53958485, compound

Product 1

HCID 59654766HCID 59654766, compound

Procedure

Diispropylethylamine (300 μl) was added to a stirred solution of 5-phenyl-furan-2-carboxylic acid (73.5 mg, 0.39 mmol) and ethyl-4-aminophenyl acetate (70 mg, 0.39 mmoles) in N,N-dimethylformamide (10 ml). O-(7-Azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (200 mg, 0.52 mmoles) was added and the solution was stirred at room temperature for 72 hours. The solvent was evaporated, the residue was dissolved in dichloromethane and washed with water, 10% aqueous sodium carbonate, 1 M aqueous hydrochloric acid and finally dried (MgSO4). After evaporation of the solvent, the residue was triturated with cyclohexane and dried to afford (1) (82 mg) as a gum. LC/MS System A; Rt=3.80 mins, m/z (ES+)=350 (M+H for C21H19NO4).

Workup

  1. customThe solvent was evaporated
  2. dissolutionthe residue was dissolved in dichloromethane
  3. washwashed with water, 10% aqueous sodium carbonate, 1 M aqueous hydrochloric acid
  4. dry with materialfinally dried (MgSO4)
  5. customAfter evaporation of the solvent
  6. customthe residue was triturated with cyclohexane
  7. customdried

Sources & evidence

ORD record
ord-25c1f5b303d842f8a720dbfd6df24669
Source dataset
uspto-grants-2008_02
Patent number
US07326732B2

Reaction notes

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