HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl chlorophosphate → 4-[3-chloro-5-(trifluoromethyl)phenyl]-N-diethoxyphosphoryl-2-pyrimidin-2-yl-5-(trifluoromethyl)pyrazol-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl chlorophosphate | HCID 13139 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(7-Chloro-1,3-benzodioxol-5-yl)-2-pyrimidin-2-yl-5-(trifluoromethyl)pyrazol-3-amine | HCID 90010064 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-[3-chloro-5-(trifluoromethyl)phenyl]-N-diethoxyphosphoryl-2-pyrimidin-2-yl-5-(trifluoromethyl)pyrazol-3-amine | HCID 72189647 | 23% |
Reaction Steps
To a mixture of 4-(7-chloro-1,3-benzodioxol-5-yl)-2-pyrimidin-2-yl-5-(trifluoromethyl)pyrazol-3-amine (0.766 g, 2.00 mmol) and NaH (0.054 g, 2.20 mmol) in tetrahydrofuran at 0° C. is added diethyl chlorophosphate (0.414 g, 2.40 mmol). The mixture is allowed to reach room temperature (20-25° C.) and further stirred for 12 hours. The reaction was diluted with water and extracted with ethyl acetate; the organic layer separated and further washed with water and then dried and concentrated. The residue was re-crystallized with a mixture of ethyl acetate and petrole ether to give the title compound (125 mg; 12%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09174967B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-df0409b2864a4bf3afccdb0552921cec |
| Source note | uspto-grants-2015_11 |