HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874978Generated: October 26, 2026
Diisopropylethylamine → N-({4-Chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-5-methyl-2H-1,2,3-triazole-4-carboxamide
https://huagongshe.com/reaction/1874978
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-methyl-2H-1,2,3-triazole-4-carboxylic acid | HCID 4436040 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | 3-{[3-(Aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-chlorobenzonitrile | HCID 59451392 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-({4-Chloro-3-[(3-chloro-5-cyanophenyl)oxy]-2-fluorophenyl}methyl)-5-methyl-2H-1,2,3-triazole-4-carboxamide | HCID 59451546 | 28.2% |
Reaction Steps
HATU (0.092 g, 0.241 mmol) was added to a solution of 3-{[3-(aminomethyl)-6-chloro-2-fluorophenyl]oxy}-5-chlorobenzonitrile (0.050 g, 0.161 mmol), 5-methyl-2H-1,2,3-triazole-4-carboxylic acid (0.022 g, 0.177 mmol) and DIPEA (0.042 mL, 0.241 mmol) in DMF (2 mL). The resulting solution was stirred overnight. The reaction mixture was partitioned between water and EtOAc. The organic layer was separated, dried over MgSO4 and evaporated to a residue. Purification was accomplished by reverse-phase HPLC (water/acetonitrile with 0.1% TFA) to afford the title compound (0.0191 g, 28%) as a white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 10.51 (s, 1H), 7.79 (d, 1H), 7.69 (t, 1H), 7.46-7.51 (m, 2H), 7.44 (d, 1H), 7.30 (t, 1H), 4.36 (d, 2H), 2.15 (s, 3H). LCMS: m/z 420.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08304419B2 |
|---|
| Source dataset | uspto-grants-2012_11 |
|---|
| ORD ID | ord-7547c531244546b4b4dab2b9796d1684 |
|---|
| Source note | uspto-grants-2012_11 |
|---|