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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1974631Generated: November 1, 2026

HCID 15751520, compound → HCID 15751521, compound

https://huagongshe.com/reaction/1974631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 15751520HCID 15751520—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 15751521HCID 1575152172%

Reaction Steps

tert-Butyl 4-[2-(benzyloxy)-5-cyclopropyl-8-fluoro-1,2,3,5-tetrahydro-1,3-dioxopyrimido[1,6-a]benzimidazol-7-yl]-1-piperazinecarboxylate (981 mg, 1.87 mmol) is dissolved in ethanol (250 ml) and hydrogenated with 5 percent palladium/carbon (200 mg) under hydrogen at normal pressure. The palladium/carbon is filtered off and washed with dimethylformamide (100 ml) at 100°. The combined filtrates are evaporated under reduced pressure. The residue is recrystallized from dimethylformamide. There are obtained 619 mg (72%) of tert-butyl 4-[5-cyclopropyl-8-fluoro-1,2,3,5-tetrahydro-2-hydroxy-1,3-dioxopyrimido[1,6-a]benzimidazol-7-yl]-1-piperazinecarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05283248
Source datasetuspto-grants-1994_02
ORD IDord-f63270a1bff14769bd74ed3e507195ef
Source noteuspto-grants-1994_02