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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364969Generated: October 31, 2026

2,4,6-Trimethylpyridine → HCID 58866206, compound

https://huagongshe.com/reaction/1364969

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrimethylpyridineHCID 7953—
ReactantEthyl 3-(4-aminophenyl)acrylateHCID 97826—
ReactantHOAtHCID 181649—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 21105263HCID 21105263—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 58866206HCID 5886620654%

Reaction Conditions

Temperature60 °C

Reaction Steps

5-(2-trimethylsilanyl-ethoxycarbonylamino)-1,3-dioxane-5-carboxylic acid from above (0.050 g, 0.17 mmol), ethyl-4-aminocinnamate (0.036 g, 0.19 mmol), HATU (0.098 g, 0.26 mmol), HOAt (0.035 g, 0.26 mmol) and 2,4,6-collidine (0.062 mL, 0.51 mmol) were combined in anhydrous DMSO (1 mL). The solution was warmed to 60° C. and stirred for 6 h before another 1.5 equivalents of HATU was added and stirring was continued for another 2 hours to ensure complete consumption of the acid. The reaction mixture was diluted with dichloromethane and washed with 1N HCl (×2). The organic phase was dried with MgSO4, filtered and concentrated. The residue was subjected to flash chromatography to afford 0.043 g (54%) of the protected amide derivative as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888363B2
Source datasetuspto-grants-2011_02
ORD IDord-4a423f7c5c5041afa6cb3983cab69ff7
Source noteuspto-grants-2011_02