Acetic Acid → HCID 58494145, compound

HRID 1942591Notes

Reaction equation

HRID 1942591 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:12]2[S:16][C:15]([C:17]3[C:18]([CH2:25][CH3:26])=[C:19]([CH:22]=[CH:23][CH:24]=3)[CH:20]=O)=[N:14][N:13]=2)[CH:5]=[CH:6][C:7]=1[O:8][CH:9]([CH3:11])[CH3:10].[NH:27]1[CH2:30][CH:29]([CH2:31]C(OC)=O)[CH2:28]1.[C:36]([O-])(=[O:38])C.[Na+].CC(O)=[O:43]>CO>[Cl:1][C:2]1[CH:3]=[C:4]([C:12]2[S:16][C:15]([C:17]3[C:18]([CH2:25][CH3:26])=[C:19]([CH2:20][N:27]4[CH2:28][CH:29]([C:31]([O:38][CH3:36])=[O:43])[CH2:30]4)[CH:22]=[CH:23][CH:24]=3)=[N:14][N:13]=2)[CH:5]=[CH:6][C:7]=1[O:8][CH:9]([CH3:10])[CH3:11]

Participants

6

Reactant 4

HCID 176Acetic AcidHCID 517045Sodium AcetateHCID 53408531Methyl (azetidin-3-yl)acetateHCID 584940093-(5-{3-Chloro-4-[(1-methylethyl)oxy]phenyl}-1,3,4-thiadiazol-2-yl)-2-ethylbenzaldehyde

Product 1

HCID 58494145HCID 58494145, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

To a solution of 3-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,3,4-thiadiazol-2-yl)-2-ethylbenzaldehyde (D11) (43 mg) and methyl 3-azetidinylacetate (92 mg) in methanol (10.00 mL) stirred at room temperature was added sodium acetate (45.6 mg) and AcOH (0.032 mL). The reaction mixture was stirred at room temperature for 10 min. Then the solvent was removed by evaporation. The residue was dissolved in dichloromethane (DCM) (10 mL), and sodium triacetoxyborohydride (70.7 mg) was added. Stirring continued for 2 h. Water was added to quench the reaction, and DCM was removed by evaporation. The mixture was extracted by EA 3 times. The combined organic solution was washed by brine, dried over anhydrous Na2SO4. The dried solution was filtered and concentrated to give crude methyl 1-{[3-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,3,4-thiadiazol-2-yl)-2-ethylphenyl]methyl}-3-azetidinecarboxylate (D13) (54 mg). MS (ES): C25H28ClN3O3S requires 485. found 486.0 (M+H+).

Workup

  1. customThen the solvent was removed by evaporation
  2. dissolutionThe residue was dissolved in dichloromethane (DCM) (10 mL)
  3. additionsodium triacetoxyborohydride (70.7 mg) was added
  4. stirringStirring
  5. waitcontinued for 2 h
  6. additionWater was added
  7. customto quench
  8. customthe reaction, and DCM
  9. customwas removed by evaporation
  10. extractionThe mixture was extracted by EA 3 times
  11. washThe combined organic solution was washed by brine
  12. dry with materialdried over anhydrous Na2SO4
  13. filtrationThe dried solution was filtered
  14. concentrationconcentrated

Sources & evidence

ORD record
ord-038096f84c8c4f06a92861507b5817a1
Source dataset
uspto-grants-2013_03
Patent number
US08389508B2

Reaction notes

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