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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620699Generated: October 31, 2026

Dimethylamine → HCID 86678861, compound

https://huagongshe.com/reaction/1620699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantDiisopropylethylamineHCID 81531—
Reactant(2S)-2-(((tert-butoxy)carbonyl)amino)-3-methoxypropanoic acidHCID 7016354—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 86678861HCID 8667886192.6%

Reaction Steps

To a solution of N-(tert-butoxycarbonyl)-O-methyl-L-serine (2.00 g), 50% aqueous dimethylamine solution (0.987 g) and N-ethyl-N-(1-methylethyl)propan-2-amine (2.36 g) in DMF (20 mL) was added O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (3.82 g) under ice-cooling. The reaction mixture was stirred at room temperature overnight. The reaction mixture was added to water, and the mixture was extracted with ethyl acetate. The organic layer was separated, washed with water and saturated brine, dried over anhydrous magnesium sulfate, concentrated under reduced pressure. The residue was purified by silica gel column chromatography (NH, ethyl acetate/hexane) to give the title compound (2.08 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772277B2
Source datasetuspto-grants-2014_07
ORD IDord-2532679f478c4f9596eb07851dabdccf
Source noteuspto-grants-2014_07