HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114145Generated: October 30, 2026
1-Hydroxybenzotriazole → HCID 69200824, compound
https://huagongshe.com/reaction/2114145
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| 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 | 5'-amino-N-(cyclopropylmethyl)-2'-methyl-1,1'-biphenyl-4-carboxamide | HCID 11300488 | — |
| Reactant | 6-(4-Fluorophenyl)-2-pyrazinecarboxylic acid | HCID 69203963 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 69200824 | HCID 69200824 | 91% |
Reaction Steps
5′-Amino-N-(cyclopropylmethyl)-2′-methyl-1,1′-biphenyl4-carboxamide (75 mg, 0.27 mmol), 6-(4fluorophenyl)pyrazine-2-carboxylic acid (58.4 mg, 0.27 mmol), HATU (101.5 mg, 0.27 mmol), HOBT (36 mg, 0.27 mmol) and DIPEA (140 μl, 0.80 mmol) in DMF (3 ml) were stirred at room temperature for 18 h. The reaction was diluted with ethyl acetate (150 ml), washed with hydrochloric acid (0.5M, 2×20ml), aqueous sodium hydrogen carbonate (20 ml) and dried (magnesium sulphate). Evaporation of the solvents under vacuum gave N-(4′-{[(cyclopropylmethyl)amino]carbonyl}-6-methyl-1,1′-biphenyl-3-yl)-6-(4-fluorophenyl)pyrazine-2-carboxamide (117 mg, 91%). NMR; δH [2H6]—DMSO 10:64,(1H, s), 9.52,(1H, s), 9.20,(1H, s), 8.63,(1H, t), 8.54,(2H, m), 7.95,(2H, d), 7.88,(1H, dd), 7.78,(1H, d), 7.48,(2H, d), 7.42,(2H, t), 7.35,(1H, d), 3.17,(2H, t), 2.23,(3H, s), 1.05,(1H, m), 0.24,(2H, m). LCMS: retention time 3.65 min, MH+481.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07432289B2 |
|---|
| Source dataset | uspto-grants-2008_10 |
|---|
| ORD ID | ord-20df778a3d514a86bb3c683e41ab07ba |
|---|
| Source note | uspto-grants-2008_10 |
|---|