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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1729807Generated: November 1, 2026

HCID 21500250, compound → HCID 21500251, compound

https://huagongshe.com/reaction/1729807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21500250HCID 21500250—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21500251HCID 21500251—

Reaction Steps

A mixture of 39.6 parts of methyl 4-(4-chloro-2-nitrophenylamino)-2-methyl-1-piperidinecarboxylate and 450 parts of tetrahydrofuran is hydrogenated at 40 lbs./sq. inch and at room temperature with 2 parts of raney-nickel catalyst. After the calculated amount of hydrogen is taken up, the catalyst is filtered off. The filtrate is evaporated, yielding methyl 4-(2-amino-4-chlorophenylamino)-2-methyl-1-piperidinecarboxylate as an oily residue.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03989707
Source datasetuspto-grants-1976_11
ORD IDord-83e97be998c542e3a83f0db94c0d9164
Source noteuspto-grants-1976_11