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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882270Generated: October 31, 2026

N,N-Dimethylethylenediamine → HCID 66571166, compound

https://huagongshe.com/reaction/882270

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylethylenediamineHCID 66053—
ReactantDiisopropylethylamineHCID 81531—
ReactantLithiumHCID 3028194—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 70976470HCID 70976470—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 66571166HCID 6657116641%

Reaction Steps

To a solution of 2-(4-((2S,4R)-1-acetyl-4-((5-cyanopyridin-2-yl)amino)-2-methyl-1,2,3,4-tetrahydroquinolin-6-yl)phenyl)acetic acid, lithium salt (for a preparation see Intermediate 9)(125 mg, 0.284 mmol) and N1,N1-dimethylethane-1,2-diamine (32.5 mg, 0.369 mmol) in DMF (3 mL) were added HATU (162 mg, 0.426 mmol) and DIPEA (0.149 mL, 0.851 mmol). The resulting mixture was stirred at room temperature for 2 h, the reaction mixture was diluted with EtOAc and water. The layers were separated and the aqueous phase was extracted with EtOAc (×3). The combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated in vacuo. The crude residue was dissolved in 1:1 MeOH/DMSO and was purified by MDAP (formate). The appropriate fractions were combined and concentrated in vacuo to give 2-(4-((2S,4R)-1-acetyl-4-((5-cyanopyridin-2-yl)amino)-2-methyl-1,2,3,4-tetrahydroquinolin-6-yl)phenyl)-N-(2-(dimethylamino)ethyl)acetamide (59 mg, 41%) as a colourless oil. LCMS (Formate, 2 min), Rt=0.65 min, MH+=511.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993554B2
Source datasetuspto-grants-2015_03
ORD IDord-3ba9d8754f274b54bbeb2bc7c5bff0b6
Source noteuspto-grants-2015_03