HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591291Generated: October 30, 2026
Potassium Carbonate → HCID 178454211, compound
https://huagongshe.com/reaction/591291
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Phenyl-1,3-dioxan-5-yl 4-methylbenzenesulfonate | HCID 3089973 | — |
| Reactant | di-tert-butyl (4S)-N-(tert-butoxycarbonyl)-4-(4-hydroxybenzyl)-L-glutamate | HCID 70957078 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178454211 | HCID 178454211 | — |
Reaction Steps
To 349 mg (0.75 mmol) of di-tert-butyl (4S)—N-(tert-butoxycarbonyl)-4-(4-hydroxy-benzyl)-L-glutamate (Example 1 b) in 15 mL NA-dimethylformamide were added 138 mg (1.0 mmol) of potassium carbonate and 332 mg (1.0 mmol) of 2-phenyl-1,3-dioxan-5-yl 4-methylbenzenesulfonate (Studii si Cercetari de Chimie (1960), 8, 187-99.) and the resulting suspension was heated for 2 h at 100° C. in a microwave oven. The reaction mixture was then filtered, the solvent evaporated and the residue was taken up in DMSO. The crude product obtained in this manner was chromatographed on a PrepCon® C-18 reversed phase column using a water/acetonitrile gradient (35/65 to 0/100), and the appropriate fractions were combined and concentrated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09238631B2 |
|---|
| Source dataset | uspto-grants-2016_01 |
|---|
| ORD ID | ord-b1a48950e7fe4f98b8090e4d2e7b37d1 |
|---|
| Source note | uspto-grants-2016_01 |
|---|