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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2362316Generated: November 1, 2026

1,2-Ethanediamine, N1,N1,N2-trimethyl- → HCID 71293445, compound

https://huagongshe.com/reaction/2362316

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Ethanediamine, N1,N1,N2-trimethyl-HCID 67338—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 71293468HCID 71293468—
SolventDimethylformamideHCID 6228—
ProductHCID 71293445HCID 7129344574.4%

Reaction Steps

Intermediate 17 (48 mg, 0.09 mmol) was dissolved in DMF (1 mL), and then diisopropylethylamine (48 μL, 0.28 mmol) and HATU (39 mg, 0.10 mmol) were added. The reaction mixture was stirred at RT for 30 minutes and then N,N,N-trimethylethylenediamine (36 μL, 0.28 mmol) was added. After 3 hours of stirring at RT, another portion of HATU was added (10 mg, 0.03 mmol), and stirring was continued for 1 hour. The reaction mixture was partitioned between EtOAc and water. The organic layer was separated, and the aqueous layer further extracted with EtOAc. The combined organic layers were washed with brine, dried (Na2SO4) and evaporated in vacuo. The resulting residue was purified by silica gel chromatography eluting with a gradient of 0-10% (2M NH3 in MeOH) in DCM to give the title compound as a white solid (40 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691826B2
Source datasetuspto-grants-2014_04
ORD IDord-aaa48861358c4af8b436b939f75f435d
Source noteuspto-grants-2014_04