Hydrochloric Acid → HCID 53234689, compound

HRID 1476167Notes

Reaction equation

HRID 1476167 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH2:9][C:10]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[OH:18])=[O:11])[CH:5]=[C:6]([F:8])[CH:7]=1.[C:19](OC(=O)CC)(=O)[CH2:20][CH3:21].Cl>C(N(CC)CC)C>[F:1][C:2]1[CH:3]=[C:4]([C:9]2[C:10](=[O:11])[C:12]3[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=3)[O:18][C:19]=2[CH2:20][CH3:21])[CH:5]=[C:6]([F:8])[CH:7]=1

Participants

5

Reactant 3

HCID 313Hydrochloric AcidHCID 31263Propionic anhydrideHCID 60209055HCID 60209055, compound

Product 1

HCID 53234689HCID 53234689, compoundYield 72%

Reagents, catalysts & solvents 1

HCID 8471TriethylamineSolvent

Procedure

Intermediate 70 (2.0 g, 8.08 mmoles) was taken in a RB flask and to this triethylamine (20 ml) and propionic anhydride (3.26 g, 25.2 mmoles) were added and the mixture was refluxed for 24 h. After cooling to RT, the reaction mixture was acidified by the addition of 1N HCl solution, extracted with ethyl acetate, washed with sodium bicarbonate solution, dried with sodium sulphate and concentrated. The crude product was purified by column chromatography with ethyl acetate:petroleum ether to afford the title compound as off-colourless liquid (1.65 g, 72% yield). 1H-NMR (δ ppm, DMSO-d6, 400 MHz): δ 8.05(dd, J=7.9,1.2Hz, 1H), 7.8 (dt, J=8.5,1.4Hz, 1H), 7.68(d, J=8.4Hz, 1H), 7.51(t, J=7.8Hz, 1H), 7.30(tt, J=7.2,2.2Hz, 1H), 7.07(d, J=6.1Hz, 2H), 2.58(q, J=7.5Hz, 1H), 1.21(t, J=7.6Hz, 3H).

Workup

  1. additionwere added
  2. temperaturethe mixture was refluxed for 24 h
  3. extractionextracted with ethyl acetate
  4. washwashed with sodium bicarbonate solution
  5. dry with materialdried with sodium sulphate
  6. concentrationconcentrated
  7. customThe crude product was purified by column chromatography with ethyl acetate

Sources & evidence

ORD record
ord-bf6054d2bdcb4a68861b306ad58d7b1e
Source dataset
uspto-grants-2015_04
Patent number
US09018375B2

Reaction notes

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