HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716188Generated: October 31, 2026
HCID 71007327, compound → HCID 71007334, compound
https://huagongshe.com/reaction/716188
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 71007327 | HCID 71007327 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 71007334 | HCID 71007334 | 111.7% |
Reaction Steps
tert-butyl (3-(3-aminopyridin-4-yl)-5-methylphenyl) carbamate. A solution of tert-butyl (3-methyl-5-(3-nitropyridin-4-yl)phenyl)carbamate (198 mg, 0.60 mmol) in EtOH (5 mL) and EtOAc (5 mL) was degassed by bubbling N2 (g) through the solution for 10 min. Pd/C (10 wt %, 64 mg, 0.060 mmol) was added. A gas bag with a 3-way stopcock filled with H2 was attached to the flask. The flask was evacuated under vacuum and then back-filled with H2 (3×). The mixture was stiffed overnight at RT. The solution was degassed by bubbling N2 (g) through the solution for 10 min and was then filtered through celite. The solution was concentrated to afford tert-butyl (3-(3-aminopyridin-4-yl)-5-methylphenyl)carbamate (200 mg, 0.67 mmol, 111% yield) as an off-white foam. MS (ESI, pos. ion) m/z: 300.0 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09187486B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-886ab991c7fe4d059be079548838d921 |
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| Source note | uspto-grants-2015_11 |
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