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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1974635Generated: October 27, 2026

HCID 56620044, compound → HCID 56637805, compound

https://huagongshe.com/reaction/1974635

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 56620044HCID 56620044—
SolventDimethylformamideHCID 6228—
SolventPalladiumHCID 23938—
ProductHCID 56637805HCID 5663780584%

Reaction Steps

Benzyl [(S)-1-[[4-[2-(benzyloxy)-5-cyclopropyl-8-fluoro-1,2,3,5-tetrahydro-1,3-dioxopyrimido[1,6-a]benzimidazol-7-yl]-1-piperazinyl]carbonyl]ethyl]carbamate (127 mg, 0.194 mmol) is dissolved in DMF (15 ml) and hydrogenated over 5 percent Pd/C. After completion of the reduction the catalyst is filtered off and the filtrate is evaporated. The residue is taken up in methanol (50 ml) and treated with active charcoal. After filtering off the charcoal the filtrate is concentrated to a volume of 25 ml. The separated crystals are filtered off. There are obtained 62 mg (84%) of 7-(4-L-alanyl-1-piperazinyl)-5-cyclopropyl-8-fluoro-2-hydroxypyrimido[1,6-a]benzimidazole-1,3(2H,5H)-dione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05283248
Source datasetuspto-grants-1994_02
ORD IDord-b700337c10794be98e3f0b8b60429868
Source noteuspto-grants-1994_02