HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → 1-Tert-butoxycarbonyl-4-methyl-5-(2-imidazolinylamino)benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | N-(1-tert-butoxycarbonyl-4-methyl-5-benzimidazolyl)-N'-2-aminoethylthiourea | HCID 21472715 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Tert-butoxycarbonyl-4-methyl-5-(2-imidazolinylamino)benzimidazole | HCID 67727353 | — |
Reaction Steps
A mixture of N-(1-tert-butoxycarbonyl-4-methyl-5-benzimidazolyl)-N'-2-aminoethylthiourea (2.89 g) and mercuric acetate (3.32 g) in methanol (200 mL)/chloroform (100 mL) is stirred at room temperature for 2 hours. The resulting black mixture is filtered on Celite and the filtrate rotary evaporated. The residue is purified by flash chromatography on a short pad of silica gel, eluting with 10% methanol/chloroform containing 1% ammonium hydroxide. The product-containing fractions are collected and rotary evaporated to afford 1-tert-butoxycarbonyl-4-methyl-5-(2-imidazolinylamino)benzimidazole as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05541210 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-4aa2ce5c0bba4d3e919ab8f28a22b727 |
| Source note | uspto-grants-1996_07 |