HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 178513229, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 1-Oxo-3-(4-trifluoromethyl-phenyl)-1,2-dihydro-pyrrolo[1,2-a]pyrazine-6-carbonitrile | HCID 72714943 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178513229 | HCID 178513229 | 70% |
Reaction Steps
A mixture of 1-oxo-3-(4-trifluoromethyl-phenyl)-1,2-dihydro-pyrrolo[1,2-a]pyrazine-6-carbonitrile (Example 2), (0.05 g, 0.16 mmol), hydroxylamine hydrochloride (15 mg, 0.22 mmol) and N,N-diisopropylethylamine (86.4 μL, 0.49 mmol,) was stirred in methylene chloride (0.5 mL), methanol (0.5 mL) and N,N-dimethylformamide (0.2 mL) at 45° C. for 2 d. At this time, the resulting solids were collected by filtration to afford N-hydroxy-1-oxo-3-(4-trifluoromethyl-phenyl)-1,2-dihydro-pyrrolo[1,2-a]pyrazine-6-carboxamidine (40 mg, 70%) as an off-white solid. 1H NMR (methanol-d4) δ ppm 7.83 (q, J=8.4 Hz, 4H), 7.73 (s, 2H), 7.37 (s, 1H). LC-MS calcd. for C15H12F3N4O2 [(M+H)+] 337, obsd. 337.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08841299B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-498ad876749b4faf813b54f96f693472 |
| Source note | uspto-grants-2014_09 |