HuagongsheHuagongshe Chemistry Print Report · For research reference only
Guanidine Hydrochloride → HCID 178513101, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | HCID 86607187 | HCID 86607187 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178513101 | HCID 178513101 | 57% |
Reaction Steps
To a solution of guanidine hydrochloride in anhydrous MeOH (1.5 ml) was added powder NaOEt (80 mg. 1.17 mmol). After 10 min stirring at room temperature, the reaction mixture was treated with tert-butyl [2-(2-furylmethyl)-5-phenyl-1H-pyrrol-1-yl]acetate. After 5 h stirring at 55° C., the reaction mixture was cooled and quenched with H2O (5 ml), diluted with EtOAc (15 ml). The organic layer was separated and the aqueous was extracted with EtOAc (2×15 ml). The combined organic extracts were washed with H2O (15 ml), brine (15 ml), dried (Na2SO4) and concentrated. The crude material was purified by chromatography (silica gel; EtOAc/2M NH3 in MeOH: 97/3) to give the titled compound (73 mg, 57%) as a solid: mp 80-82° C.; MS (−) ES, 321 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07488832B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-1717e5acb8024c68ad19993ae06c43f9 |
| Source note | uspto-grants-2009_02 |