HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,1,1-Trifluoro-2-iodoethane → HCID 71534973, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,1,1-Trifluoro-2-iodoethane | HCID 67709 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 71534972 | HCID 71534972 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 71534973 | HCID 71534973 | 21.2% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
A suspension of 6-(6-(1-methyl-1H-pyrazol-4-yl)-[1,2,4]triazolo[4,3-a]pyridin-3-ylthio)-3-(piperazin-1-yl)quinoline (Example 27—see in Table below) (12 mg, 0.027 mmol), 1,1,1-trifluoro-2-iodoethane (56.9 mg, 0.271 mmol) and DIPEA (17.5 mg, 0.136 mmol) in DMF (1 mL) was sealed in a microwave vial and heated at 120° C. for 6 hours. The solvent was removed and the residue was purified by prep-HPLC to give the title compound as yellow solid (3 mg, yield 20%). [Method 1C]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09062045B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-a021db1bbb1b40dc82eec87ecaa1f40c |
| Source note | uspto-grants-2015_06 |