p-Toluenesulfonic acid → HCID 135626367, compound

HRID 2412995Notes

Reaction equation

HRID 2412995 reaction equation
[NH2:1][C:2]1[C:3]([NH:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[C:15]([C:17]2[CH:22]=[CH:21][CH:20]=[C:19]([Cl:23])[CH:18]=2)=O)=[N:4][CH:5]=[CH:6][CH:7]=1.C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1>[Cl:23][C:19]1[CH:18]=[C:17]([C:15]2[C:10]3[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=3[NH:8][C:3]3[N:4]=[CH:5][CH:6]=[CH:7][C:2]=3[N:1]=2)[CH:22]=[CH:21][CH:20]=1

Participants

4

Reactant 2

HCID 6101p-Toluenesulfonic acidHCID 15586656{2-[(3-Aminopyridin-2-yl)amino]phenyl}(3-chlorophenyl)methanone

Product 1

HCID 135626367HCID 135626367, compound

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

A mixture of 14 g (0.0433 mole) of [2-[(3-amino-2-pyridinyl)amino]phenyl](3-chlorophenyl)-methanone and 0.3 g of para toluene sulfonic acid in 500 ml of toluene were heated at reflux overnight using a Dean-Stark trap to collect water. At the end of the reflux time, some of the toluene (ca 250 ml) was distilled off and the hot solution was filtered. Pet. ether (30°-60° C.) was added to the cloud point. The solution was refrigerated overhight and filtered to give, after air drying, 10 g (76%) gold colored crystals. A portion was recrystallized from isopropyl alcohol-isopropyl ether, m.p. 160°-160.5° C.

Workup

  1. temperaturewere heated
  2. temperatureat reflux overnight
  3. customto collect water
  4. distillationAt the end of the reflux time, some of the toluene (ca 250 ml) was distilled off
  5. filtrationthe hot solution was filtered
  6. additionPet. ether (30°-60° C.) was added to the cloud point
  7. filtrationfiltered
  8. customto give
  9. customafter air drying
  10. customA portion was recrystallized from isopropyl alcohol-isopropyl ether, m.p. 160°-160.5° C.

Sources & evidence

ORD record
ord-54fda1b64d57429792ef7a4a69102025
Source dataset
uspto-grants-1985_01
Patent number
US04495183

Reaction notes

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