HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 18400133, compound → HCID 178432209, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 18400133 | HCID 18400133 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178432209 | HCID 178432209 | — |
Reaction Steps
A mixture of N-(1-t-butoxycarbonyl-2,4-dimethyl-5-benzimidazolyl)-N′-2-aminoethylthiourea (1.33 g, 3.66 mmol) and mercuric acetate (1.45 g, 4.54 mmol) in methanol (150 mL) is stirred at room temperature for 1 hour. The resulting black mixture is filtered on Celite with a methanol wash of the solids. The filtrate is rotary evaporated and the residue is purified by flash chromatography on a short pad of silica gel, eluting with 10% methanol/chloroform containing 1% of ammonium hydroxide. The product-containing fractions are collected and rotary evaporated to afford 2,4-dimethyl-5-(2-imidazolinylamino)benzimidazole as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06486190B1 |
| Source dataset | uspto-grants-2002_11 |
| ORD ID | ord-adb2593a0a524d12a05feee60979b4e2 |
| Source note | uspto-grants-2002_11 |