HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793014Generated: October 26, 2026
2,3,4-Trifluorobenzoic acid → 3,4-difluoro-2-{2-fluoro-4-[3-(tetrahydro-2H-pyran-2-yloxy)-1-propynyl]anilino}benzoic acid
https://huagongshe.com/reaction/1793014
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3,4-Trifluorobenzoic acid | HCID 302932 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 2-fluoro-4-[3-(tetrahydro-2H-pyran-2-yloxy)-1-propynyl]aniline | HCID 22025637 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3,4-difluoro-2-{2-fluoro-4-[3-(tetrahydro-2H-pyran-2-yloxy)-1-propynyl]anilino}benzoic acid | HCID 22025655 | — |
Reaction Steps
2,3,4-Trifluorobenzoic acid and 2-fluoro-4-[3-(tetrahydro-2H-pyran-2-yloxy)-1-propynyl]aniline were reacted in the presence of LiHMDS solution in THF by the general procedure of Example 1, Step B. After workup, followed by purification by chromatography on silica gel (50% EtOAc/PE as eluant), 3,4-difluoro-2-{2-fluoro-4-[3-(tetrahydro-2H-pyran-2-yloxy)-1-propynyl]anilino}benzoic acid was isolated as a cream-yellow solid (68%); m.p. (Et2O/hexane) 164–166° C. 1H NMR [400 MHz, (CD3)2SO] δ 13.60 (v br s, 1 H), 9.27 (br s, 1 H), 7.83 (ddd, J=8.2, 6.1, 1.9 Hz, 1 H), 7.36 (dd, J=12.0, 1.7 Hz, 1 H), 7.21–7.11 (m, 2 H), 6.96 (td, J=8.8, 5.5 Hz, 1 H), 4.80 (br s, 1 H), 4.47 (d, J=16.0 Hz, 1 H), 4.38 (d, J=16.0 Hz, 1 H), 3.79–3.71 (m, 2H), 3.51–3.45 (m, 2 H), 1.77–1.61 (m, 2 H), 1.56–1.44 (m, 4 H). Anal. calcd. for C21H18F3NO4: C, 62.2; H, 4.5; N, 3.5. Found C, 62.5; H, 4.4; N, 3.6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07078438B2 |
|---|
| Source dataset | uspto-grants-2006_07 |
|---|
| ORD ID | ord-0ff016bab27144549569c92e42e28f21 |
|---|
| Source note | uspto-grants-2006_07 |
|---|