HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 11314561, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Butanamine, 2-methyl- | HCID 68986 | — |
| Reactant | HCID 178512266 | HCID 178512266 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11314561 | HCID 11314561 | 49% |
Reaction Steps
A solution of N-[3,5-bis(trifluoromethyl)phenyl]-N'-cyano-O-phenylisourea (0.78 mmol, 290 mg), tert-amylamine (0.85 mmol, 0.100 ml) and triethylamine (0.85 mmol, 0.119 ml) in acetonitrile (2 ml) was stirred for 25 h at 75° C. followed by work-up as described in EXAMPLE 5, b) to give the title compound (140 mg, 46%) as white crystals. Mp 149-150° C.; EI SP/MS: 366 (M+); 1H-NMR (CDCl3): δ 0.85 (t, 3H),1.35 (s, 6H), 1.75 (q, 2H), 4.65 (br s,1H), 7.70 (br s, 3H), 8.95 ppm (br s, 1H); MA calc for C15H16F6N4. 0.15 H2O: C, 49.37%; H, 4.57%; N, 14.76%. Found: C, 49.72%; H, 4.56%; N, 14.76%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06147098 |
| Source dataset | uspto-grants-2000_11 |
| ORD ID | ord-cd602964cb844c90a9765d03636eea8a |
| Source note | uspto-grants-2000_11 |