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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631811Generated: October 26, 2026

Oxalyl chloride → HCID 71811871, compound

https://huagongshe.com/reaction/631811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant3'-O-ethyl-N,N-diisopropylphosphoramiditeHCID 195451—
Reactant4,4,4-Trifluorocrotonic acidHCID 5709614—
Reactant(2-Aminoethyl)(4-methyl-5-nitro(2-pyridyl))amineHCID 22142401—
CatalystDichloromethaneHCID 6344—
SolventDichloromethaneHCID 6344—
ProductHCID 71811871HCID 718118715.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321724B2
Source datasetuspto-grants-2016_04
ORD IDord-67b4bac13a5d43cf849258dd613a5efc
Source noteuspto-grants-2016_04