HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → HCID 89077758, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 58312744 | HCID 58312744 | — |
| Reactant | HCID 89077759 | HCID 89077759 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 89077758 | HCID 89077758 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
The crude material from Step 2, furan-2-yl(piperazin-1-yl)methanimine hydrochloride (16.3 mg, 0.076 mmol) was diluted in DMSO (Volume: 0.75 mL) and added to (Z)-5-((2-(methylsulfonyl)pyrimidin-4-yl)methylene)thiazolidine-2,4-dione (19.4 mg, 0.068 mmol) in a 2-dram vial. The reaction solution was then treated with N-ethyl-N-isopropylpropan-2-amine (50 mg, 0.387 mmol) and then shaken at 100° C. for 16 h. The reaction was then purified by RP-HPLC using TFA as the modifier to provide (Z)-5-((2-(4-(furan-2-yl(imino)methyl)piperazin-1-yl)pyrimidin-4-yl)methylene)thiazolidine-2,4-dione.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08901145B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-e03993f2891d489aad4e9ba6a5e3744b |
| Source note | uspto-grants-2014_12 |