HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571315Generated: November 1, 2026
2-Methoxyethylamine → HCID 86681723, compound
https://huagongshe.com/reaction/571315
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Methoxyethylamine | HCID 8018 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 86681722 | HCID 86681722 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86681723 | HCID 86681723 | 52% |
Reaction Steps
To a solution of benzyl 2-(5-(N-(2-bromoethyl)methylsulfonamido)-1,3-dioxoisoindolin-2-yl)acetate (0.300 g, 0.606 mmol) in acetonitrile (6 ml), K2CO3 (0.126 g, 0.908 mmol) and 2-methoxyethanamine (0.079 ml, 0.908 mmol) were added, and the resulting mixture was heated under MW irradiation for 1 hour at 130° C. The insoluble inorganic salts were filtered off and the filtrate was evaporated to dryness. The crude was purified by flash chromatography on silica gel column (DCM:MeOH=95:5) affording benzyl 2-(5-(N-(2-(2-methoxyethylamino)ethyl)methylsulfonamido)-1,3-dioxoisoindolin-2-yl)acetate (0.154 g, 0.315 mmol, 52.0% yield, MS/ESI+ 490.0 [MH]+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09024027B2 |
|---|
| Source dataset | uspto-grants-2015_05 |
|---|
| ORD ID | ord-43cb1c0dd6b840c5afa3f7060a8dae9e |
|---|
| Source note | uspto-grants-2015_05 |
|---|