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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672844Generated: October 30, 2026

HCID 86643706, compound → HCID 67352368, compound

https://huagongshe.com/reaction/1672844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86643706HCID 86643706—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 67352368HCID 6735236872%

Reaction Steps

(S)-4-Tert-butoxycarbonyl-1-[3-(9-ethylamino-6-oxo-2,3,3a,4-tetrahydro-1H,6H-5,8,10,10b-tetraazabenzo[e]azulen-5-yl)phenyl]piperazine-1-oxide (0.338 g, 0.645 mmol) obtained in Step 2 was dissolved in ethanol (10 mL), and the mixture was stirred for 1.5 hours under a stream of hydrogen gas after adding 10% palladium-on-carbon (137 mg, 0.0646 mmol). The mixture was filtered through sellite, and the filtrate was concentrated to give (S)-5-[3-(4-tert-butoxycarbonylpiperazine-1-yl)phenyl]-9-ethylamino-1,2,3,3a,4,5-hexahydro-5,8,10,10b-tetraazabenzo[e]azulen-6-one (0.235 g, 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998954B2
Source datasetuspto-grants-2011_08
ORD IDord-41f1401687964a21ab81db1bb87b6f82
Source noteuspto-grants-2011_08