HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 22727943, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | N-Methylcyclohexylamine | HCID 7514 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | N-(6-oxo-5,6-dihydro-phenanthridin-2-yl)-chloroacetamide | HCID 9814438 | — |
| Product | HCID 22727943 | HCID 22727943 | — |
Reaction Steps
Prepared from the compound of Example 2 and N-methylcyclohexylamine. To a solution of 2-chloro-N-(5,6-dihydro-6-oxo-2-phenanthridinyl)-acetamide (45 mg) in N,N-dimethylformamide (10 mL) was added potassium phosphate (68 mg) and N-methylcyclohexylamine (0.025 mL). The solution stirred at room temperature for 5 hours followed by evaporation of the solvent. The light brown product was washed with water and filtered (30 mg). 1H-NMR (300 MHz, DMSO-d6), 11.69 (br s, 1H), 9.76 (br s, 1H), 8.65 (s, 1H), 8.34 (t, 2H), 7.87 (m, 2H), 7.66 (t, 1H), 7.32 (t, 1H), 3.18 (s, 2H), 2.34 (s, 3H), 1.80 (m, 4H), 1.60 (m, 2H), 1.23 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06723733B2 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-e5e58ce656cb4c6fb484c93e8df5cc21 |
| Source note | uspto-grants-2004_04 |