Triethylamine → N-[2-hydroxy-5-(trifluoromethyl)phenyl]-3 (methoxymethyl)isonicotinamide

HRID 2094501Notes

Reaction equation

HRID 2094501 reaction equation
[NH2:1][C:2]1[CH:7]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:5]=[CH:4][C:3]=1[OH:12].[CH3:13][O:14][CH2:15][C:16]1[CH:24]=[N:23][CH:22]=[CH:21][C:17]=1[C:18](O)=[O:19].CN([P+](ON1N=NC2C=CC=CC1=2)(N(C)C)N(C)C)C.F[P-](F)(F)(F)(F)F.C(N(CC)CC)C>O.CN(C=O)C>[OH:12][C:3]1[CH:4]=[CH:5][C:6]([C:8]([F:9])([F:10])[F:11])=[CH:7][C:2]=1[NH:1][C:18](=[O:19])[C:17]1[CH:21]=[CH:22][N:23]=[CH:24][C:16]=1[CH2:15][O:14][CH3:13]

Participants

7

Procedure

A mixture of 0.40 g of 2-amino-4-(trifluoromethyl)phenol, 0.38 g of 3-methoxymethyl isonicotinic acid, 1.30 g of BOP reagent, 0.30 g of triethylamine, and 20 ml of DMF was stirred at room temperature for four hours. Water was added to the reaction mixture, and the reaction mixture was extracted with ethyl acetate twice. The combined organic layers were washed with a saturated sodium chloride solution, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to give 0.64 g of N-[2-hydroxy-5-(trifluoromethyl)phenyl]-3 (methoxymethyl)isonicotinamide.

Workup

  1. extractionthe reaction mixture was extracted with ethyl acetate twice
  2. washThe combined organic layers were washed with a saturated sodium chloride solution
  3. dry with materialdried over anhydrous magnesium sulfate
  4. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-d4e3b05e62144db2b767228397850663
Source dataset
uspto-grants-2013_05
Patent number
US08445522B2

Reaction notes

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