HuagongsheHuagongshe Chemistry Print Report · For research reference only
Oxalyl chloride → HCID 71811871, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3'-O-ethyl-N,N-diisopropylphosphoramidite | HCID 195451 | — |
| Reactant | 4,4,4-Trifluorocrotonic acid | HCID 5709614 | — |
| Reactant | (2-Aminoethyl)(4-methyl-5-nitro(2-pyridyl))amine | HCID 22142401 | — |
| Catalyst | Dichloromethane | HCID 6344 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 71811871 | HCID 71811871 | 5.1% |
Reaction Steps
(E)-4,4,4-Trifluorobut-2-enoic acid (32 mg, 0.23 mmol) was dissolved in dichloromethane (0.5 ml containing one drop of dimethyl formamide), oxalyl chloride was added (23 μl, 0.23 mmol) and the solution was stirred at room temperature for 15 minutes. This solution was added to a solution of N-(4-methyl-5-nitro-2-pyridyl)ethane-1,2-diamine (29 mg, 0.15 mmol) and EDIPA (70 μl, 0.5 mmol) in anhydrous dichloromethane (2 ml) and the resulting mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure and the resulting residue was purified by preparative HPLC (Waters XBridge, gradient of water containing 0.1% NH3 and 10% to 100% acetonitrile) to yield 2.4 mg of a solid (0.0076 mmol, 5% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321724B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-67b4bac13a5d43cf849258dd613a5efc |
| Source note | uspto-grants-2016_04 |