Dimethylformamide → N-Methoxy-N-methyl-4-(5-trifluoromethyl-isoxazol-3-yl)-benzamide

HRID 572264Notes

Reaction equation

HRID 572264 reaction equation
[F:1][C:2]([F:18])([F:17])[C:3]1[O:7][N:6]=[C:5]([C:8]2[CH:16]=[CH:15][C:11]([C:12]([OH:14])=O)=[CH:10][CH:9]=2)[CH:4]=1.Cl.NO.C([N:24]([CH2:27]C)CC)C.C1CCC(N=C=NC2CCCCC2)CC1.CN([CH:47]=[O:48])C>ClCCl.CN(C1C=CN=CC=1)C>[CH3:47][O:48][N:24]([CH3:27])[C:12](=[O:14])[C:11]1[CH:10]=[CH:9][C:8]([C:5]2[CH:4]=[C:3]([C:2]([F:1])([F:18])[F:17])[O:7][N:6]=2)=[CH:16][CH:15]=1

Participants

8

Reactant 5

HCID 6228DimethylformamideHCID 8471TriethylamineHCID 10868DicyclohexylcarbodiimideHCID 443297Hydroxyamine hydrochlorideHCID 576061124-(5-(Trifluoromethyl)isoxazol-3-yl)benzoic acid

Product 1

HCID 57606119N-Methoxy-N-methyl-4-(5-trifluoromethyl-isoxazol-3-yl)-benzamideYield 74%

Reagents, catalysts & solvents 2

HCID 142844-(Dimethylamino)pyridineCatalystHCID 6344DichloromethaneSolvent

Procedure

A solution of 4-(5-Trifluoromethyl-isoxazol-3-yl)-benzoic acid (Preparative Example 11, 1.024 g, 4.0 mmol) in dichloromethane (14 mL) at 0-5° C. was treated with DMF (2 mL) followed by DMAP (50 mg), hydroxylamine hydrochloride (468 mg, 4.8 mmol), triethylamine (458 μL, 4.8 mmol), and DCC (990 mg, 4.8 mmol). The reaction was allowed to warm to room temperature and stirred 16 hr then evaporated in vacuo. The crude material was then chromatogrphed on silica gel with EtOAc/hexanes (40%) as eluant to afford product as a colorless solid (890 mg, 74%). 1H NMR (CDCl3) 3.40 (s, 3H), 3.57 (s, 3H), 7.06 (s, 3), 7.82 (d, J=8.3, 2H), 7.88 (d, J=8.8, 2H). 13C NMR 33.7, 61.4, 103.7, 118.0 (q, J=460), 127.1, 129.3, 129.4, 136.6, 159.7 (q, J=42), 162.2, 169.0. 19F NMR −64.6. LC/MS 6.01 min, [M+1]+ 301.

Workup

  1. customthen evaporated in vacuo

Sources & evidence

ORD record
ord-fbf089e983844569ad0fe1a02fffb2e7
Source dataset
uspto-grants-2015_05
Patent number
US09029397B2

Reaction notes

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