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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388281Generated: October 30, 2026

Water → 4-[4-(3-nitro-benzenesulfonyl)-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl]-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/388281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPyridineHCID 1049—
Reactant3-Nitrobenzenesulfonyl chlorideHCID 8476—
Reactant4-(3,4-dihydro-2H-benzo[1,4]oxazin-8-yl)-piperazine-1-carboxylic acid tert-butyl esterHCID 20765686—
SolventDichloromethaneHCID 6344—
Product4-[4-(3-nitro-benzenesulfonyl)-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl]-piperazine-1-carboxylic acid tert-butyl esterHCID 20765685102.2%

Reaction Steps

3-Nitro-benzenesulfonyl chloride (122.9 mg, 0.55 mmol) was added in small portions under nitrogen to an ice-cold solution of 4-(3,4-dihydro-2H-benzo[1,4]oxazin-8-yl)-piperazine-1-carboxylic acid tert-butyl ester (161 mg, 0.504 mmol) and pyridine (88 mg, 1.11 mmol) in dichlormethane (2 mL). After 0.5 hour at ambient temperature, water was added. The organic phase was separated, washed with saturated aqueous solution of sodium bicarbonate (20 mL), dried (Na2SO4) and concentrated to give 4-[4-(3-nitro-benzenesulfonyl)-3,4-dihydro-2H-benzo[1,4]oxazin-8-yl]-piperazine-1-carboxylic acid tert-butyl ester as an oil (260 mg). MS: MH+=505.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08377931B2
Source datasetuspto-grants-2013_02
ORD IDord-5dae263d2a79402c91336ec8dd7d636d
Source noteuspto-grants-2013_02