HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Hydroxybenzotriazole → HCID 44231565, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 260252-88-8 | HCID 18946299 | — |
| Reactant | HCID 57875825 | HCID 57875825 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 44231565 | HCID 44231565 | 30.1% |
Reaction Steps
HOBt (60 mg, 0.43 mmol), DIPEA (141 mg, 1.09 mmol), EDCI.HCl (84 mg, 0.43 mmol), 3-cyano-phenyl)-piperazin-1-yl-methanone hydrochloride (110 mg, 0.439 mmol) were added to a stirred solution of N-biphenyl-4-yl-2-fluoro-malonamic acid (100 mg, 0.36 mmol) in DMF (2.0 mL) and the resulting mixture was stirred at the ambient temperature overnight. The mixture was then diluted with water and the product was extracted with ethyl acetate. The organics were washed with brine and concentrated to afford 51 mg (29.65%) of N-Biphenyl-4-yl-3-[4-(3-cyano-benzoyl)-piperazin-1-yl]-2-fluoro-3-oxo-propionamide. LCMS: 471.18 (M+1)+, 95.1%, 1H NMR (DMSO-d6): δ 8.3 (s, 1H), 7.8-7.3 (m, 13H), 4.3-3.7 (m, 3H), 3.7-3.3 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08039463B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-a6fdfe3ca7424d82847cd445a4e4ddc0 |
| Source note | uspto-grants-2011_10 |