Sulfuric Acid → 4-Trifluoromethyl-6-(4-trifluoromethyl-phenyl)-pyridazin-3-ylamine

HRID 1293731Notes

Reaction equation

HRID 1293731 reaction equation
COC1C=CC(C[NH:8][C:9]2[N:10]=[N:11][C:12]([C:19]3[CH:24]=[CH:23][C:22]([C:25]([F:28])([F:27])[F:26])=[CH:21][CH:20]=3)=[CH:13][C:14]=2[C:15]([F:18])([F:17])[F:16])=CC=1.OS(O)(=O)=O>>[F:18][C:15]([F:16])([F:17])[C:14]1[CH:13]=[C:12]([C:19]2[CH:24]=[CH:23][C:22]([C:25]([F:28])([F:27])[F:26])=[CH:21][CH:20]=2)[N:11]=[N:10][C:9]=1[NH2:8]

Participants

3

Conditions

Temperature
5 °C

Procedure

(4-Methoxy-benzyl)-[4-trifluoromethyl-6-(4-trifluoromethyl-phenyl)-pyridazin-3-yl]-amine (example C.26 step 8) (6.48 g, 15 mmol) was added portionwise at 5° C. to conc. H2SO4 (d 1.83, 17.0 mL, 303 mmol).The deep purple solution was stirred for 5 min at 5° C. then the cooling bath was removed and stirring was continued for further 60 min at 23° C. The mixture was poured onto ice, made alkaline with 32% NaOH-sol., saturated with solid NaCl and extracted with THF and TBME, dried the organic layer over MgSO4. Removal of the solvent in vacuum left the title compound as a light yellow solid (4.44 g, 95%), which was used without further purification. MS (ISP) 308.1 [(M+H)+]; mp 186–190° C.

Workup

  1. customthe cooling bath was removed
  2. stirringstirring
  3. waitwas continued for further 60 min at 23° C
  4. additionThe mixture was poured onto ice
  5. extraction, saturated with solid NaCl and extracted with THF and TBME
  6. dry with materialdried the organic layer over MgSO4
  7. customRemoval of the solvent in vacuum
  8. waitleft the title compound as a light yellow solid (4.44 g, 95%), which
  9. customwas used without further purification

Sources & evidence

ORD record
ord-526337b9463c45d58dca151ace5ea43f
Source dataset
uspto-grants-2007_07
Patent number
US07238808B2

Reaction notes

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