HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1878324Generated: November 1, 2026
HCID 66878228, compound → HCID 66877986, compound
https://huagongshe.com/reaction/1878324
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 66878228 | HCID 66878228 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 66877986 | HCID 66877986 | 67.7% |
Reaction Steps
N-tert-Butyl-3((4-(4-nitrobenzoyl)piperazin-1-yl)methyl)benzamide (0.56 g, 1.31 mmol) was dissolved In methanol (10 mL) at room temperature. Raney 2800 nickel (−1mL of an aqueous suspension) was added and the grey suspension was stirred vigorously. A balloon of hydrogen was attached to the flask via a three-way stopcock and hydrogen was allowed to slowly flow through the system for 1 minute. The flask was sealed under 1 atmosphere of hydrogen and vigorous stirring continued for 1 hour. The balloon was removed and the flask was flushed with argon. The suspension was gravity-filtered over fluted paper and washed with methanol. The filtrate was concentrated to a crude foam/glass and silica chromatography (70-90% ethyl acetate in n-hexanes with 1-3% methanol, followed by 1-6% methanol in dichloromethane) gave the title compound (0.35 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08314091B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-48c21cc7d2264242b1ddc6fee441b1b5 |
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| Source note | uspto-grants-2012_11 |
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