HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716576Generated: November 2, 2026
4-Nitrophenyl 2,2-diethoxypropanoate → HCID 68510828, compound
https://huagongshe.com/reaction/1716576
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Nitrophenyl 2,2-diethoxypropanoate | HCID 13807233 | — |
| Reactant | 1,1-Dimethylethyl 4-[(2-amino-4-methylphenyl)amino]-1-piperidinecarboxylate | HCID 58852288 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 68510828 | HCID 68510828 | 62% |
Reaction Steps
4-(2-Amino-4-methyl-phenylamino)-piperidine-1-carboxylic acid tert-butyl ester (400 mg, 1.31 mmol), p-nitrophenyl 2,2-diethoxyproprionate (1.00 g, 3.50 mmol), and DMAP (1.00 g, 8.2 mmol) were combined in acetonitrile (3 mL) and heated in an oil bath at 80° C. for 2 h. The mixture was cooled, diluted with diethyl ether (100 mL), washed once each with saturated aqueous NH4Cl and water, three times with 5% aqueous sodium hydroxide solution, once with brine and dried over anhydrous MgSO4 and concentrated under reduced pressure. The residue was adsorbed on a silica gel pad, and the pad was eluted with 25% ethyl acetate in hexanes to give 4-[2-(2,2-diethoxy-propionylamino)-4-methyl-phenylamino]-piperidine-1-carboxylic acid tert-butyl ester (550 mg, 0.81 mmol, 62%) of a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07803816B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-44aa94696a0c49c28e957422a891ee39 |
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| Source note | uspto-grants-2010_09 |
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