HuagongsheHuagongshe Chemistry Print Report · For research reference only
4,4-Difluoro-1-(4-trifluoromethylphenyl)butane-1,3-dione → HCID 11350219, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4,4-Difluoro-1-(4-trifluoromethylphenyl)butane-1,3-dione | HCID 18920369 | — |
| Reactant | HCID 178422940 | HCID 178422940 | — |
| Product | HCID 11350219 | HCID 11350219 | 79% |
Reaction Steps
Reaction of 4,4-difluoro-1-(4-trifluoromethyl-phenyl)-butane-1,3-dione (133 mg, 0.5 mmol), prepared from commercially available 4-trifluoromethyl-acetophenone according to general procedure A, and 3-amino-4-(2-methyl-4-pyridinyl)-pyrazole [prepared from 4-cyanomethyl-2-methyl-pyridine, as described in Bioorg. Med. Chem. Lett. 12 (2002) 3537-3541] (87 mg, 0.5 mmol) according to general procedure B yielded the title compound as a yellow solid (159 mg, 79%). MS (ISP) 405.4 [(M+H)+]; mp 213° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07514443B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-b4813604cf954bf5aefa26cff59c709b |
| Source note | uspto-grants-2009_04 |