Acetic Acid → HCID 57503360, compound

HRID 1669808Notes

Reaction equation

HRID 1669808 reaction equation
[CH3:1][C:2]1[O:3][C:4]2[C:9]([C:10](=[O:12])[CH:11]=1)=[CH:8][CH:7]=[CH:6][C:5]=2[CH:13]=O.O=[C:16]([CH3:24])[CH2:17][C:18]([O:20][CH2:21][CH2:22][CH3:23])=[O:19].[NH2:25][C:26]([CH3:37])=[CH:27][C:28]([C:30]1[CH:35]=[CH:34][C:33]([F:36])=[CH:32][CH:31]=1)=[O:29].C(O)(=O)C>CC(O)C>[CH3:24][C:16]1[NH:25][C:26]([CH3:37])=[C:27]([C:28](=[O:29])[C:30]2[CH:35]=[CH:34][C:33]([F:36])=[CH:32][CH:31]=2)[CH:13]([C:5]2[CH:6]=[CH:7][CH:8]=[C:9]3[C:4]=2[O:3][C:2]([CH3:1])=[CH:11][C:10]3=[O:12])[C:17]=1[C:18]([O:20][CH2:21][CH2:22][CH3:23])=[O:19]

Participants

6

Reactant 4

HCID 176Acetic AcidHCID 74507Propyl acetoacetateHCID 133748832-Methyl-4-oxo-4H-chromene-8-carbaldehydeHCID 67342452HCID 67342452, compound

Product 1

HCID 57503360HCID 57503360, compound

Reagents, catalysts & solvents 1

HCID 3776IsopropanolSolvent

Procedure

110 mg (0.54 mmol) of 2-methyl-4-oxo-4H-chromene-8-carbaldehyde are dissolved with 78 mg (0.54 mmol) of n-propyl 3-oxobutanoate, 97 mg (0.54 mmol) of 3-amino-1-(4-fluorophenyl)but-2-en-1-one and 6 μl (0.05 mmol) of acetic acid in 10 ml of 2-propanol and heated under reflux under argon for 30 h. The solvent is removed in vacuo, and the residue is purified by preparative HPLC. 228 mg (87% of theory) of the title compound are obtained as a yellow solid.

Workup

  1. temperatureheated
  2. temperatureunder reflux under argon for 30 h
  3. customThe solvent is removed in vacuo
  4. customthe residue is purified by preparative HPLC

Sources & evidence

ORD record
ord-de58744297e44a589229fad15569f551
Source dataset
uspto-grants-2011_08
Patent number
US07989633B2

Reaction notes

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