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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479326Generated: October 31, 2026

Diisopropylethylamine → HCID 86682236, compound

https://huagongshe.com/reaction/1479326

Reaction equation

Participants

RoleNameHCIDCharge
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—
ReactantAmmonia methanolHCID 21705897—
ReactantHCID 86699641HCID 86699641—
SolventChloroformHCID 6212—
ProductHCID 86682236HCID 8668223685.4%

Reaction Steps

The resulting 3-(bis(2-((Z)-octadec-9-enyloxy)ethyl)amino)propanoic acid (85 mg, 0.125 mmol) was dissolved in chloroform (3 mL), and stirred overnight at room temperature after adding 0(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (HATU; Aldrich; 95 mg, 0.251 mmol), a 7 mol/L ammonia methanol solution (0.090 mL, 0.627 mmol), and diisopropylethylamine (0.109 mL, 0.627 mmol). The aqueous layer was extracted with ethyl acetate after adding a saturated sodium bicarbonate aqueous solution to the reaction mixture. The organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure after filtration. The resulting residue was purified by silica gel column chromatography (chloroform/methanol=100/0 to 88/12) to give compound 84 (72.3 mg, 85.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09408914B2
Source datasetuspto-grants-2016_08
ORD IDord-059ef0adf99048fda023e52b0ff2b873
Source noteuspto-grants-2016_08