HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 453194Generated: October 26, 2026
Water → 4-Fluoro-5-(2-hydroxymethyl-pyrimidin-4-yloxy)-2-methyl-indole-1-carboxylic acid (3-trifluoromethyl-phenyl)-amide
https://huagongshe.com/reaction/453194
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | acetic acid 4-[4-fluoro-2-methyl-1-(3-trifluoromethyl-phenylcarbamoyl)-1H-indol-5-yloxy]-pyrimidin-2-ylmethyl ester | HCID 59394198 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-Fluoro-5-(2-hydroxymethyl-pyrimidin-4-yloxy)-2-methyl-indole-1-carboxylic acid (3-trifluoromethyl-phenyl)-amide | HCID 59394538 | — |
Reaction Steps
Potassium carbonate (289 mg, 2.09 mmol) is added to a solution of acetic acid 4-[4-fluoro-2-methyl-1-(3-trifluoromethyl-phenylcarbamoyl)-1H-indol-5-yloxy]-pyrimidin-2-ylmethyl ester (1.05 g, 2.09 mmol) in MeOH (40 mL) at 23° C. The resulting mixture is stirred at 23° C. for 1 h. Saturated aqueous NH4Cl (50 mL) and water (20 mL) are added and the mixture is extracted with EtOAc (3×50 mL). The organic layers are combined, washed with brine (30 mL), dried (Na2SO4), and concentrated. The residue is purified by silica gel chromatography (10-100% EtOAc/heptane) to provide 4-fluoro-5-(2-hydroxymethyl-pyrimidin-4-yloxy)-2-methyl-indole-1-carboxylic acid (3-trifluoromethyl-phenyl)-amide. MS (ESI) m/z 461.0 (M+1); 1H NMR (400 MHz, DMSO-d6) δ ppm 11.02 (s, 1 H) 8.69 (d, J=5.56 Hz, 1 H) 8.12 (s, 1 H) 7.91 (s, 1 H) 7.66 (t, J=7.96 Hz, 1 H) 7.52 (t, J=8.34 Hz, 2 H) 7.17 (dd, J=8.84, 7.83 Hz, 1 H) 7.05 (d, J=5.56 Hz, 1 H) 6.63 (s, 1 H) 5.14 (t, J=6.19 Hz, 1 H) 4.38 (d, J=6.32 Hz, 2 H) 2.59 (s, 3 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08492393B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-ffba00771c2044e6ae455c689aa2dc4d |
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| Source note | uspto-grants-2013_07 |
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