Hydrochloric Acid → HCID 66877087, compound

HRID 1364948Notes

Reaction equation

HRID 1364948 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9](=[O:18])[C:10]2[CH:15]=[CH:14][C:13]([C:16]#[N:17])=[CH:12][CH:11]=2)=[CH:4][C:3]=1[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][N:20]=1.Cl.[CH2:26]([OH:28])[CH3:27]>>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][C:9]([C:10]2[CH:11]=[CH:12][C:13]([C:16](=[NH:17])[O:28][CH2:26][CH3:27])=[CH:14][CH:15]=2)=[O:18])=[CH:4][C:3]=1[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][N:20]=1

Participants

4

Reactant 3

HCID 313Hydrochloric AcidHCID 702EthanolHCID 66877347N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-cyanobenzamide

Product 1

HCID 66877087HCID 66877087, compound

Conditions

Temperature
70 °C

Procedure

4-Chloro-3-(pyridin-2-yl)aniline (687 mg, 3.36 mmol) was dissolved in dichloromethane (8.0 ml) and THF (8.0 ml), treated with pyridine (0.33 ml, 4.0 mmol), and cooled to 0° C. 4-Cyanobenzoyl chloride (612 mg, 3.7 mmol) was added and the reaction was stirred for 1.0 hour. The reaction was diluted with dichloromethane and methanol was added to dissolve all solids. The solution was washed with water once, brine once, dried with MgSO4, and evaporated to an orange solid which was purified by silica gel flash column chromatography (50% ethyl acetate/50% hexanes) to afford 908 mg of N-(4-chloro-3-(pyridin-2-yl)phenyl)-4-cyanobenzamide as a yellow solid. N-(4-Chloro-3-(pyridin-2-yl)phenyl)-4-cyanobenzamide (500 mg, 1.5 mmol) was slurried in ethanol (75 ml) and heated until just dissolved. The solution was cooled in an ice bath, and saturated with HCl gas. The solution was heated briefly to 70° C. to dissolve precipitated solids, cooled in an ice bath, and resaturated with HCl gas. The solution was then stored at 0° C. for 18 hours. The solution was saturated again with HCl gas, heated to 70° C. until all solids dissolved, cooled to 0° C., resaturated with HCl gas, and stored at 0° C. for 18 hours. Finally, nitrogen gas was bubbled through the solution for 1.0 hour, and the solution was evaporated to dryness. The residue was dissolved in methanol, treated with MP-carbonate (2.57 g) and stirred 30 min. The solution was filtered to afford a neutral, methanolic solution of ethyl 4-(4-chloro-3-(pyridin-2-yl)phenylcarbamoyl)benzimidate, which was diluted with enough methanol to make a 0.075 M solution.

Workup

  1. temperatureheated
  2. dissolutionuntil just dissolved
  3. temperatureThe solution was cooled in an ice bath
  4. dissolutionto dissolve
  5. customprecipitated solids
  6. temperaturecooled in an ice bath
  7. temperatureheated to 70° C. until all solids
  8. dissolutiondissolved
  9. temperaturecooled to 0° C.
  10. waitstored at 0° C. for 18 hours
  11. customFinally, nitrogen gas was bubbled through the solution for 1.0 hour
  12. customthe solution was evaporated to dryness
  13. dissolutionThe residue was dissolved in methanol
  14. additiontreated with MP-carbonate (2.57 g)
  15. filtrationThe solution was filtered

Sources & evidence

ORD record
ord-1bc58e3e4595443c9c2090be41fc3f5b
Source dataset
uspto-grants-2011_02
Patent number
US07888364B2

Reaction notes

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