HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Ether → HCID 86636984, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Cyclobutylamine | HCID 75645 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Tris(1,1-dimethylethyl) 2-(2,6-dichloro-5-fluoro-4-pyrimidinyl)-1,1,2-hydrazinetricarboxylate | HCID 58000755 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86636984 | HCID 86636984 | — |
Reaction Steps
To a solution of tris(1,1-dimethylethyl)2-(2,6-dichloro-5-fluoro-4-pyrimidinyl)-1,1,2-hydrazinetricarboxylate (0.497 g, 1.0 mmol) in DMF (5 mL) at room temperature was added diisopropylethylamine (0.19 mL, 1.10 mmol) followed immediately by commercially available cyclobutylamine (0.085 mL, 1.0 mmol). The reaction was stirred for 4 days, then ether was added, and the mixture was washed with water and the aqueous layer was back extracted. The combined organics were dried (Na2SO4), concentrated in vacuo, and azeotroped once with MeOH to provide tris(1,1-dimethylethyl)2-[2-chloro-6-(cyclobutylamino)-5-fluoro-4-pyrimidinyl]-1,1,2-hydrazinetricarboxylate as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07893056B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-103b8768fdde4b28a3da1ae52a96cb78 |
| Source note | uspto-grants-2011_02 |