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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983824Generated: October 31, 2026

8-(4-Tert-butoxycarbonyl-piperazin-1-yl)-6-chloro-2,3-dihydro-benzo[1,4]oxazine-4-carboxylic acid benzyl ester → 4-(3,4-dihydro-2H-benzo[1,4]oxazin-8-yl)-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/983824

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-(4-Tert-butoxycarbonyl-piperazin-1-yl)-6-chloro-2,3-dihydro-benzo[1,4]oxazine-4-carboxylic acid benzyl esterHCID 20765682—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product4-(3,4-dihydro-2H-benzo[1,4]oxazin-8-yl)-piperazine-1-carboxylic acid tert-butyl esterHCID 2076568684%

Reaction Steps

A solution of 8-(4-tert-butoxycarbonyl-piperazin-1-yl)-6-chloro-2,3-dihydro-benzo[1,4]oxazine-4-carboxylic acid benzyl ester (640 mg, 1.32 mmol) in ethanol (10 mL) was hydrogenated at 50 psi in the presence of palladium on carbon for 12 hours. The catalyst was removed by filtration, and the filtrate was concentrated to give 4-(3,4-dihydro-2H-benzo[1,4]oxazin-8-yl)-piperazine-1-carboxylic acid tert-butyl ester as a light yellow solid (350 mg, 84%). MS: MH+=320.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06867204B2
Source datasetuspto-grants-2005_03
ORD IDord-ac427649059044e88cb5bcf4cee49df4
Source noteuspto-grants-2005_03