HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 70016891, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1-Trityl-4-(4-cyanobenzyl)imidazole | HCID 15837533 | — |
| Reactant | HCID 18779697 | HCID 18779697 | — |
| Product | HCID 70016891 | HCID 70016891 | — |
Reaction Steps
The bromide from Step 2 (0.154 g, 0.516 mmol) and 4-(1-trityl-1H-imidazol-4-ylmethyl)-benzonitrile (0.22 g, 0.516 mmol) in CH3CN (2 mL) were heated at 55° C. After 18 hr methanol (3 mL) was added and the reaction was heated at reflux for 3 hrs, cooled and the solvent evaporated in vacuo. The residue was partitioned between sat. NaHCO3 and CH2Cl2 and extracted with CH2Cl2. The organic extracts were dried (Na2SO4) and evaporated in vacuo. The residue was chromatographed (silica gel, MeOH: CH2Cl2 5:95 as eluent) to afford the free base which was converted to the hydrochloride salt to afford the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05939439 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-79f86f0ce7bb4c0cb769ca2f5de86a82 |
| Source note | uspto-grants-1999_08 |