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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172683Generated: November 2, 2026

N,N-Dimethylethylenediamine → HCID 71230972, compound

https://huagongshe.com/reaction/2172683

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylethylenediamineHCID 66053—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-[5-(Trifluoromethyl)-1,2,4-oxadiazol-3-yl]benzoic acidHCID 10491405—
Reactant(1-Cyano-2-ethoxy-2-oxoethylidenaminooxy)dimethylamino-morpholino-carbenium hexafluorophosphateHCID 75951468—
SolventDichloromethaneHCID 6344—
ProductHCID 71230972HCID 7123097279.9%

Reaction Steps

To a suspension of Intermediate 12b (1 g, 3.87 mmol) in DCM (20 ml) was added COMU (1.891 g, 4.26 mmol) and DIPEA (0.812 ml, 4.65 mmol). The yellow solution was stirred for 2 min at rt and turned red. 2-Dimethylaminoethylamine (0.518 ml, 4.65 mmol) was added and the reaction mixture was stirred at reflux for 1 hr. After cooling to rt, the mixture was washed with water, saturated aqueous NH4Cl and extrated with EtOAc. The organic layer was dried over Na2SO4 and the solvent was removed in vacuo. The crude product was purified by flash chromatography (ISCO CombiFlash Rf, 120 g silicagel; A=dichloromethane, B=DCM:7N NH3 in MeOH (9:1), 2% hold for 5 min, gradient to 50% B over 15 min). Fractions containing the product where combined to yield 1.355 g. The final product (1.015 g) was obtained after crystallisation from heptane as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056843B2
Source datasetuspto-grants-2015_06
ORD IDord-939cd4ccdd5a47ceae382044c987c40e
Source noteuspto-grants-2015_06