HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formate → HCID 178425605, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formate | HCID 283 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(3-Methylphenylaminocarbonylamino)eth-1-ylamine | HCID 22138859 | — |
| Reactant | HCID 178467516 | HCID 178467516 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178425605 | HCID 178425605 | 91% |
Reaction Steps
To a solution of N-(4-ethoxy-1,1-dioxo-1,2,5-thiadiazol-3-yl)-L-tyrosine tert-butyl ester from Step A (150 mg, 0.38 mmol) and the formate salt of 2-(3-methylphenylaminocarbonylamino)eth-1-ylamine from Step B (210 mg, 0.89 mmol) in ethanol (10 mL) was added triethylamine (133 mg, 1.44 mmol). The reaction was stirred at room temperature overnight. Solvent was removed under reduced pressure and the residue purified by flash column chromatography (silica, 5% MeOH in EtOAc) to give the title compound (130 mg, 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07005433B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-c40a236245c14680869b44498f31fa30 |
| Source note | uspto-grants-2006_02 |