HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642882Generated: October 29, 2026
HCID 58592783, compound → HCID 58592820, compound
https://huagongshe.com/reaction/642882
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 58592783 | HCID 58592783 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 58592820 | HCID 58592820 | 101.1% |
Reaction Steps
In a round bottom flask under nitrogen was combined 4-[4-(3-Azido-4-nitro-benzyl)-piperazin-1-yl]-2-(4-tert-butyl-phenyl)-1H-benzoimidazole (0.19 g, 0.37 mMol), methanol (20 mL), and 5% platinum on carbon (0.145 g, 0.037 mMol). A hydrogen balloon was attached, the flask evacuated, and a hydrogen atmosphere established. After stirring for four hours, the balloon was removed, the flask purged with nitrogen, and the reaction mixture filtered thru Celite with a large excess of methanol. The solution was concentrated to dryness on a rotary evaporator to yield 170 mg (100% yield) of 4-{4-[2-(4-tert-Butyl-phenyl)-1H-benzoimidazol-4-yl]-piperazin-1-ylmethyl}-benzene-1,2-diamine as a brown oil. LC/MS (Method A), rt=0.90 mins., purity=85.9%, calculated mass=454, [M+H]+=455, [M−H]−=453.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07696210B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-5d42c42ad32a483f96363fb4a985c9dd |
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| Source note | uspto-grants-2010_04 |
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