HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 22940401, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 22940404 | HCID 22940404 | — |
| Catalyst | Water | HCID 962 | — |
| Catalyst | Sulfuric Acid | HCID 1118 | — |
| Catalyst | Diacetyloxymercury | HCID 16683746 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 22940401 | HCID 22940401 | — |
Reaction Steps
A solution of (+,−)-N-(cis-2-(3-Ethynylphenyl)-cyclopropyl)-N′-(5-chloropyrid-2-yl)-urea of Example 22(130 mg, 0.42 mmole), H2SO4 (10 drops), H2O (10 drops) and Hg(OAc)2 (100 mg) in acetic acid (4 mL) was stirred at room temperature for 30 min. The reaction mixture was then poured into an ethyl acetate and saturated K2CO3 solution. The organic layer was dried (MgSO4) and the solvent was evaporated to give a residue which was purified on silica gel using 1:1 acetone: and hexanes as the eluent providing 43 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06376492B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-be84e8343a3f407eaaf6aa4956653ab5 |
| Source note | uspto-grants-2002_04 |