HCID 57546006, compound → HCID 57545927, compound

HRID 913993Notes

Reaction equation

HRID 913993 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2([CH2:21][O:22][CH2:23][C:24]3[CH:25]=[C:26]([C:33]([F:36])([F:35])[F:34])[CH:27]=[C:28]4[C:32]=3[NH:31][N:30]=[CH:29]4)[CH2:13][CH2:12][N:11](C(OC(C)(C)C)=O)[CH2:10][CH2:9]2)=[CH:4][CH:3]=1>FC(F)(F)C(O)=O>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2([CH2:21][O:22][CH2:23][C:24]3[CH:25]=[C:26]([C:33]([F:34])([F:35])[F:36])[CH:27]=[C:28]4[C:32]=3[NH:31][N:30]=[CH:29]4)[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]2)=[CH:4][CH:3]=1

Participants

3

Reactant 1

HCID 57546006HCID 57546006, compound

Product 1

HCID 57545927HCID 57545927, compound

Reagents, catalysts & solvents 1

HCID 6422Trifluoroacetic acidSolvent

Procedure

tert-Butyl 4-(4-fluorophenyl)-4-(((5-(trifluoromethyl)-1H-indazol-7-yl)methoxy)methyl)piperidine-1-carboxylate (75 mg, 0.148 mmol) was dissolved in trifluoroacetic acid (25% in dichloromethane, 1 mL) and stirred at room temperature for 15 min. The reaction was concentrated and loaded onto a strong cation exchange cartridge in methanol. The cartridge was flushed with several volumes of methanol which were discarded. The product was eluted with 2 M ammonia in methanol and concentrated to give 59 mg (98%). 1H-NMR (CDCl3, 500 MHz) δ 8.06 (s, 1H), 7.94 (s, 1H), 7.20-7.40 (m, 3H), 7.07 (m, 2H), 4.71 (s, 2H), 3.50 (s, 2H), 3.43 (s, 2H), 2.88 (m, 2H), 2.72 (m, 2H), 2.12 (m, 2H), 1.85 (m, 2H); 13C-NMR (CDCl3, 126 MHz) δ 162.5, 160.5, 139.6, 139.5, 135.3, 128.64, 128.58, 124.7 (q, J=272 Hz), 123.2 (q, J=32 Hz), 122.9, 121.8, 120.6, 118.5 (q, J=3.8 Hz), 115.8, 115.6, 80.3, 71.6, 50.5, 42.4, 41.4, 33.7. Mass spec.: 408.09 (MH)+. Accurate mass spec.: m/z 408.1680 [MH]+, Δ=4.7 ppm.

Workup

  1. concentrationThe reaction was concentrated
  2. customThe cartridge was flushed with several volumes of methanol which
  3. washThe product was eluted with 2 M ammonia in methanol
  4. concentrationconcentrated
  5. customto give 59 mg (98%)

Sources & evidence

ORD record
ord-86bf1bf7c96d46b18c17146c0b62872a
Source dataset
uspto-grants-2011_09
Patent number
US08026257B2

Reaction notes

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