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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| Reactant | Ethyl 3-(4-aminophenyl)acrylate | HCID 97826 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 21105263 | HCID 21105263 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 58866206 | HCID 58866206 | 54% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07888363B2 |
|---|
| Source dataset | uspto-grants-2011_02 |
|---|
| ORD ID | ord-4a423f7c5c5041afa6cb3983cab69ff7 |
|---|
| Source note | uspto-grants-2011_02 |
|---|