HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 9821211, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Butanamine, 3,3-dimethyl- | HCID 520907 | — |
| Reactant | HCID 178512266 | HCID 178512266 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 9821211 | HCID 9821211 | 46% |
Reaction Steps
A solution of N-[3,5-bis(trifluoromethyl)phenyl]-N'-cyano-O-phenylisourea (0.8 mmol, 300 mg), 2-amino-3,3-dimethylbutane (0.88 mmol, 0.09 g) and triethylamine (0.88 mmol, 0.123 ml) in acetonitrile (2 ml) was stirred for 8 h at 75° C. After concentration the residue was purified by column chromatography (heptane:ethyl acetate 2:1) to give the title compound (140 mg, 46%) as white crystals. Mp 165.5-166.5° C.; EI SP/MS: 380 (M+); 1H-NMR (CDCl3): δ 0.92 (s, 9H),1.13 (d, 3H), 3.8 (m, 1H), 4.8 (br d, 1H), 7.74 (br s, 3H), 8.5 ppm (br, 1H); MA calc for C16H18F6N4 : C, 50.53%; H, 4.77%; N, 14.73%. Found: C, 50.48%; H, 4.74%; N, 14.45%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06147098 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-d5ec66115c104966a22b4e6694e20452 |
| Source note | uspto-grants-2000_11 |