HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116558Generated: October 27, 2026
N-(2-furanylmethyl) 5-nitro-2-(3-chloro-5-pyridyloxy)benzamide → N-(2-furanylmethyl) 5-amino-2-(3-chloro-5-pyridyloxy)benzamide
https://huagongshe.com/reaction/2116558
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-(2-furanylmethyl) 5-nitro-2-(3-chloro-5-pyridyloxy)benzamide | HCID 54136240 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(2-furanylmethyl) 5-amino-2-(3-chloro-5-pyridyloxy)benzamide | HCID 53712390 | 76% |
Reaction Steps
To a 0.08M solution of N-(2-furanylmethyl) 5-nitro-2-(3-chloro-5-pyridyloxy)benzamide (3.7 g, 10 mmol, prepared in Example 35.2) in MeOH was added a 50% aqueous slurry of Raney nickel (˜6 mL). Hydrogen was then bubbled through the resulting solution for one minute. The resulting mixture was stirred at ambient temperature under one atmosphere of hydrogen for 16 hr. The crude reaction mixture was filtered through a pad of Celite® and the filter cake was washed 3× with MEOH. NOTE: Raney nickel is pyrophoric and should always be kept wet with solvent during the filtration. The Raney nickel can be quenched by adding 6M aqueous HCl. The filtrate was concentrated in the presence of benzene to azeotropically remove water. The residue was purified by chromatography (1-3% MeOH in CH2Cl2) to yield 2.6 g (76%) of N-(2-furanylmethyl) 5-amino-2-(3chloro-5-pyridyloxy)benzamide as a pale brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07439242B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-f41081289dba43c5ad2a864d1948f38b |
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| Source note | uspto-grants-2008_10 |
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