Acetic Acid → HCID 178506183, compound

HRID 1486579Notes

Reaction equation

HRID 1486579 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([NH:9][C:10]2[N:14]=[C:13]([NH2:15])[NH:12][N:11]=2)[CH:5]=[C:6]([Cl:8])[CH:7]=1.[Cl:16][C:17]1[CH:18]=[C:19]([CH:22]=[CH:23][C:24]=1[C:25]([F:28])([F:27])[F:26])[CH:20]=O.C(O)(=O)C.Cl>CO>[Cl:16][C:17]1[CH:18]=[C:19]([CH:22]=[CH:23][C:24]=1[C:25]([F:26])([F:27])[F:28])[CH2:20][NH:15][C:13]1[NH:12][N:11]=[C:10]([NH:9][C:4]2[CH:5]=[C:6]([Cl:8])[CH:7]=[C:2]([Cl:1])[CH:3]=2)[N:14]=1

Participants

6

Reactant 4

HCID 176Acetic AcidHCID 313Hydrochloric AcidHCID 190312873-Chloro-4-(trifluoromethyl)benzaldehydeHCID 727146143-Amino-5-(3,5-dichloroanilino)-s-triazole

Product 1

HCID 178506183HCID 178506183, compoundYield 68%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

To a solution of N3-(3,5-dichlorophenyl)-1H-1,2,4-triazole-3,5-diamine Intermediate 2 (200 mg, 819 μmol) in MeOH (3.5 ml) was added 3-chloro-4-(trifluoromethyl)benzaldehyde (94.0 mg, 451 μmol) followed by acetic acid (36.7 mg, 35.0 μl, 611 μmol). The reaction was stirred at room temperature for 15 minutes, 2-picoline borane complex (52.6 mg, 492 μmol) was added and the stirring was continued for 4 days. The reaction mixture was poured into 0.1N HCl solution (20 ml). The resulting suspension was filtered to collect the solid. Purification by flash chromatography (silica gel, 24 g, 2% to 4% MeOH in DCM) afforded a white solid as desired product (121.4 mg, 68% yield). MS +m/z: 436 (M+H)+

Workup

  1. addition2-picoline borane complex (52.6 mg, 492 μmol) was added
  2. waitthe stirring was continued for 4 days
  3. filtrationThe resulting suspension was filtered
  4. customto collect the solid
  5. customPurification by flash chromatography (silica gel, 24 g, 2% to 4% MeOH in DCM)

Sources & evidence

ORD record
ord-8e7efd7a08f547849ef6bf09e025345d
Source dataset
uspto-grants-2016_08
Patent number
US09428469B2

Reaction notes

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