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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569986Generated: October 29, 2026

HCID 13670002, compound → HCID 13670004, compound

https://huagongshe.com/reaction/569986

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 13670002HCID 13670002—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 13670004HCID 1367000495%

Reaction Steps

Dissolved in 20 ml of ethanol was 1.0 g of the 1,4,5,6-tetrahydro-6-ethyl-5-oxo-2-(4-benzylpiperazino)pyrido[4,3-d]pyrimidine obtained in Referential Example 31, followed by an addition of 10% Pd-C. The resultant mixture was stirred at 70° C. for 2.5 hours in a hydrogen atmosphere. After removal of the catalyst by filtration, the filtrate was concentrated to obtain 0.7 g of 1,4,5,6-Tetrahydro-6-ethyl-5-oxo-2-piperazinopyrido[4,3-d]pyrimidine as crystals (yield: 95%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04734418
Source datasetuspto-grants-1988_03
ORD IDord-f4707bb5a7cd4d68aef7753c82b281be
Source noteuspto-grants-1988_03