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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981304Generated: October 30, 2026

Thiophene → Ethyl cis-4-[(5-amino-4-chloro-2-methoxybenzoyl)amino]-3-methoxy-1-piperidinecarboxylate

https://huagongshe.com/reaction/981304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiopheneHCID 8030—
ReactantHCID 67928767HCID 67928767—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
SolventMethanolHCID 887—
ProductEthyl cis-4-[(5-amino-4-chloro-2-methoxybenzoyl)amino]-3-methoxy-1-piperidinecarboxylateHCID 6792877994%

Reaction Steps

A mixture of 90.5 parts of ethyl cis-4-[(4-chloro-2-methoxy-5-nitrobenzoyl)amino]-3-methoxy-1-piperidinecarboxylate, 3 parts of a solution of thiophene in methanol 4% and 400 parts of methanol was hydrogenated at normal pressure and at 50° C. with 5 parts of platinum-on-charcoal catalyst 5%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The residue was crystallized from 2-propanol. The product was filtered off and dried, yielding 80 parts (94%) of ethyl cis-4-[(5-amino-4-chloro-2-methoxybenzoyl)amino]-3-methoxy-1-piperidinecarboxylate: mp. 142.5° C. (interm. 14).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04990521
Source datasetuspto-grants-1991_02
ORD IDord-5a421704462c4aab8f8178eddca63923
Source noteuspto-grants-1991_02