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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437664Generated: October 30, 2026

HCID 21428943, compound → HCID 21428880, compound

https://huagongshe.com/reaction/437664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21428943HCID 21428943—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventAcetic AcidHCID 176—
ProductHCID 21428880HCID 21428880—

Reaction Steps

A mixture of 6 parts of 5-chloro-2-methoxy-4-nitro-N-[2-(4-oxo-1-phenyl-1,3,8-triazaspiro[4,5] dec-8-yl)ethyl]benzamide in 150 parts of acetic acid is hydrogenated at normal pressure and at room temperature with 1 part of Raney-nickel catalyst. After the calculated amount of hydrogen is taken up, the catalyst is filtered off and the filtrate is evaporated. The residue is taken up in water and the whole is alkalized. The precipitated product is filtered off and crystallized twice from ethanol, yielding 1.7 parts of 4-amino-5-chloro-2-methoxy-N-[2-(4-oxo-1-phenyl-1,3,8-triazaspiro[4,5]-dec-8-yl)ethyl]benzamide; mp. 247.4° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04031226
Source datasetuspto-grants-1977_06
ORD IDord-0d8651c7d3e44633823e1f37e7956e3a
Source noteuspto-grants-1977_06